Linked Data
ClinVar Variation Id:
65897
dbSNP Id:
rs587778809
ExAC:
4:128859936 A / T
gnomAD v2:
4-128859936-A-T
gnomAD v3:
4-127938781-A-T
gnomAD v4:
4-127938781-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.127938781A>T , CM000666.2:g.127938781A>T | GRCh38 |
| NC_000004.11:g.128859936A>T , CM000666.1:g.128859936A>T | GRCh37 |
| NC_000004.10:g.129079386A>T | NCBI36 |
| NG_008657.1:g.32204T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296468.8:c.754+2T>A | ENSP00000296468.3:n.754+2T>A | |
| ENST00000505284.6:n.970+2T>A | ||
| ENST00000509826.2:c.698+1072T>A | ENSP00000421176.2:n.698+1072T>A | |
| ENST00000513559.6:c.472+2T>A | ENSP00000425000.2:n.472+2T>A | |
| ENST00000515130.6:c.619+2T>A | ENSP00000493056.1:n.619+2T>A | |
| ENST00000641025.1:c.754+2T>A | ENSP00000493346.1:n.754+2T>A | |
| ENST00000641092.1:c.553+3264T>A | ENSP00000493392.1:n.553+3264T>A | |
| ENST00000641133.1:c.*68+2T>A | ENSP00000493192.1:n.*68+2T>A | |
| ENST00000641134.1:c.474+2T>A | ENSP00000492925.1:n.474+2T>A | |
| ENST00000641147.1:c.304+4971T>A | ENSP00000493133.1:n.304+4971T>A | |
| ENST00000641178.1:c.619+2T>A | ENSP00000492989.1:n.619+2T>A | |
| ENST00000641186.1:c.640+2T>A | ENSP00000493347.1:n.640+2T>A | |
| ENST00000641228.1:c.553+3264T>A | ENSP00000493194.1:n.553+3264T>A | |
| ENST00000641243.1:c.609+2T>A | ENSP00000493083.1:n.609+2T>A | |
| ENST00000641264.1:c.*551+2T>A | ENSP00000492908.1:n.*551+2T>A | |
| ENST00000641332.1:c.609+2T>A | ENSP00000493397.1:n.609+2T>A | |
| ENST00000641340.1:c.698+1072T>A | ENSP00000493191.1:n.698+1072T>A | |
| ENST00000641369.1:c.250+2T>A | ENSP00000493037.1:n.250+2T>A | |
| ENST00000641393.1:c.304+4971T>A | ENSP00000493197.1:n.304+4971T>A | |
| ENST00000641397.1:c.439+4971T>A | ENSP00000493406.1:n.439+4971T>A | |
| ENST00000641434.1:c.754+2T>A | ENSP00000493279.1:n.754+2T>A | |
| ENST00000641464.1:c.449+1072T>A | ENSP00000493438.1:n.449+1072T>A | |
| ENST00000641482.1:c.754+2T>A | ENSP00000493277.1:n.754+2T>A | |
| ENST00000641503.1:c.640+2T>A | ENSP00000493304.1:n.640+2T>A | |
| ENST00000641508.1:c.698+1072T>A | ENSP00000493209.1:n.698+1072T>A | |
| ENST00000641509.1:c.439+4971T>A | ENSP00000493459.1:n.439+4971T>A | |
| ENST00000641538.1:c.600+2T>A | ||
| ENST00000641590.1:c.640+2T>A | ENSP00000493132.1:n.640+2T>A | |
| ENST00000641658.1:c.474+2T>A | ENSP00000492987.1:n.474+2T>A | |
| ENST00000641686.2:c.754+2T>A MANE Select | ENSP00000493218.2:n.754+2T>A | |
| ENST00000641690.1:c.553+3264T>A | ENSP00000492966.1:n.553+3264T>A | |
| ENST00000641695.1:c.*38+2T>A | ENSP00000493134.1:n.*38+2T>A | |
| ENST00000641742.1:c.609+2T>A | ENSP00000493315.1:n.609+2T>A | |
| ENST00000641743.1:c.754+2T>A | ENSP00000493130.1:n.754+2T>A | |
| ENST00000641748.1:c.754+2T>A | ENSP00000493330.1:n.754+2T>A | |
| ENST00000641753.1:c.581+2T>A | ||
| ENST00000641774.1:c.584+1072T>A | ENSP00000492960.1:n.584+1072T>A | |
| ENST00000641776.1:c.*306+2T>A | ENSP00000493261.1:n.*306+2T>A | |
| ENST00000641830.1:c.90+2T>A | ||
| ENST00000641843.1:c.360+2T>A | ENSP00000493174.1:n.360+2T>A | |
| ENST00000641869.1:c.59+2T>A | ||
| ENST00000641870.1:c.609+2T>A | ENSP00000493044.1:n.609+2T>A | |
| ENST00000641882.1:c.495+2T>A | ENSP00000493301.1:n.495+2T>A | |
| ENST00000641928.1:c.449+1072T>A | ENSP00000493418.1:n.449+1072T>A | |
| ENST00000641949.1:c.553+3264T>A | ENSP00000492891.1:n.553+3264T>A | |
| ENST00000642012.1:n.618+2T>A | ||
| ENST00000642034.1:c.640+2T>A | ENSP00000493285.1:n.640+2T>A | |
| ENST00000642042.1:c.754+2T>A | ENSP00000493260.1:n.754+2T>A | |
| ENST00000642078.1:c.474+2T>A | ENSP00000492885.1:n.474+2T>A | |
| ENST00000642121.1:n.91-7964T>A | ||
| ENST00000296468.7:c.754+2T>A | ENSP00000296468.3:n.754+2T>A | |
| ENST00000505284.5:n.649+2T>A | ||
| ENST00000509826.1:c.449+1072T>A | ENSP00000421176.1:n.449+1072T>A | |
| ENST00000513559.5:c.619+2T>A | ENSP00000425000.1:n.619+2T>A | |
| ENST00000515130.5:n.1200+2T>A | ||
| NM_152778.2:c.754+2T>A | NP_689991.1:n.754+2T>A | |
| XM_005262893.1:c.754+2T>A | XP_005262950.1:n.754+2T>A | |
| XM_005262896.1:c.607+2T>A | XP_005262953.1:n.607+2T>A | |
| XM_005262897.1:c.553+3264T>A | XP_005262954.1:n.553+3264T>A | |
| XM_005262898.2:c.754+2T>A | XP_005262955.1:n.754+2T>A | |
| XM_005262900.2:c.609+2T>A | XP_005262957.1:n.609+2T>A | |
| XM_011531830.1:c.640+2T>A | XP_011530132.1:n.640+2T>A | |
| XM_011531831.1:c.439+4971T>A | XP_011530133.1:n.439+4971T>A | |
| XM_011531832.1:c.640+2T>A | XP_011530134.1:n.640+2T>A | |
| XR_938717.1:n.831+2T>A | ||
| NM_001363520.1:c.553+3264T>A | NP_001350449.1:n.553+3264T>A | |
| NM_001363521.1:c.439+4971T>A | NP_001350450.1:n.439+4971T>A | |
| XM_005262898.3:c.754+2T>A | XP_005262955.1:n.754+2T>A | |
| XM_017007989.1:c.553+3264T>A | XP_016863478.1:n.553+3264T>A | |
| XM_024453981.1:c.619+2T>A | XP_024309749.1:n.619+2T>A | |
| XM_024453982.1:c.505+2T>A | XP_024309750.1:n.505+2T>A | |
| XM_024453983.1:c.304+4971T>A | XP_024309751.1:n.304+4971T>A | |
| XR_001741194.1:n.831+2T>A | ||
| XR_001741195.1:n.717+2T>A | ||
| XR_001741196.1:n.630+3264T>A | ||
| XR_001741197.1:n.686+2T>A | ||
| XR_001741198.2:n.686+2T>A | ||
| XR_001741199.1:n.686+2T>A | ||
| XR_938717.2:n.831+2T>A | ||
| NM_001363520.2:c.553+3264T>A | NP_001350449.1:n.553+3264T>A | |
| NM_001363521.2:c.439+4971T>A | NP_001350450.1:n.439+4971T>A | |
| NM_001371590.1:c.619+2T>A | NP_001358519.1:n.619+2T>A | |
| NM_001371591.1:c.754+2T>A | NP_001358520.1:n.754+2T>A | |
| NM_001371592.1:c.760+2T>A | NP_001358521.1:n.760+2T>A | |
| NM_001371593.1:c.640+2T>A | NP_001358522.1:n.640+2T>A | |
| NM_001371594.1:c.607+2T>A | NP_001358523.1:n.607+2T>A | |
| NM_001371595.1:c.472+2T>A | NP_001358524.1:n.472+2T>A | |
| NM_001371596.2:c.754+2T>A MANE Select | NP_001358525.1:n.754+2T>A | |
| NM_152778.3:c.754+2T>A | NP_689991.1:n.754+2T>A | |
| NM_152778.4:c.754+2T>A | NP_689991.1:n.754+2T>A |