Linked Data
ClinVar Variation Id:
1003
dbSNP Id:
rs118203977
gnomAD v2:
4-128851942-A-C
gnomAD v4:
4-127930787-A-C
PubMed:
PMID:17564970
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.127930787A>C , CM000666.2:g.127930787A>C | GRCh38 |
| NC_000004.11:g.128851942A>C , CM000666.1:g.128851942A>C | GRCh37 |
| NC_000004.10:g.129071392A>C | NCBI36 |
| NG_008657.1:g.40198T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296468.8:c.894T>G | ENSP00000296468.3:p.Tyr298Ter | |
| ENST00000509826.2:c.*127T>G | ENSP00000421176.2:n.*127T>G | |
| ENST00000513559.6:c.612T>G | ENSP00000425000.2:p.Tyr204Ter | |
| ENST00000515130.6:c.759T>G | ENSP00000493056.1:p.Tyr253Ter | |
| ENST00000641003.1:n.284T>G | ||
| ENST00000641025.1:c.894T>G | ENSP00000493346.1:p.Tyr298Ter | |
| ENST00000641092.1:c.693T>G | ENSP00000493392.1:p.Tyr231Ter | |
| ENST00000641133.1:c.*208T>G | ENSP00000493192.1:n.*208T>G | |
| ENST00000641146.1:n.760T>G | ||
| ENST00000641147.1:c.444T>G | ENSP00000493133.1:p.Tyr148Ter | |
| ENST00000641178.1:c.759T>G | ENSP00000492989.1:p.Tyr253Ter | |
| ENST00000641186.1:c.780T>G | ENSP00000493347.1:p.Tyr260Ter | |
| ENST00000641228.1:c.693T>G | ENSP00000493194.1:p.Tyr231Ter | |
| ENST00000641332.1:c.*59T>G | ENSP00000493397.1:n.*59T>G | |
| ENST00000641340.1:c.*127T>G | ENSP00000493191.1:n.*127T>G | |
| ENST00000641369.1:c.390T>G | ENSP00000493037.1:p.Tyr130Ter | |
| ENST00000641388.1:n.245T>G | ||
| ENST00000641393.1:c.444T>G | ENSP00000493197.1:p.Tyr148Ter | |
| ENST00000641397.1:c.579T>G | ENSP00000493406.1:p.Tyr193Ter | |
| ENST00000641434.1:c.894T>G | ENSP00000493279.1:p.Tyr298Ter | |
| ENST00000641464.1:c.*127T>G | ENSP00000493438.1:n.*127T>G | |
| ENST00000641482.1:c.894T>G | ENSP00000493277.1:p.Tyr298Ter | |
| ENST00000641508.1:c.*127T>G | ENSP00000493209.1:n.*127T>G | |
| ENST00000641509.1:c.579T>G | ENSP00000493459.1:p.Tyr193Ter | |
| ENST00000641538.1:c.709+2198T>G | ||
| ENST00000641590.1:c.780T>G | ENSP00000493132.1:p.Tyr260Ter | |
| ENST00000641658.1:c.*59T>G | ENSP00000492987.1:n.*59T>G | |
| ENST00000641686.2:c.894T>G MANE Select | ENSP00000493218.2:p.Tyr298Ter | |
| ENST00000641690.1:c.693T>G | ENSP00000492966.1:p.Tyr231Ter | |
| ENST00000641742.1:c.*59T>G | ENSP00000493315.1:n.*59T>G | |
| ENST00000641748.1:c.894T>G | ENSP00000493330.1:p.Tyr298Ter | |
| ENST00000641753.1:c.721T>G | ||
| ENST00000641774.1:c.*127T>G | ENSP00000492960.1:n.*127T>G | |
| ENST00000641830.1:c.230T>G | ||
| ENST00000641843.1:c.*59T>G | ENSP00000493174.1:n.*59T>G | |
| ENST00000641869.1:c.199T>G | ||
| ENST00000641870.1:c.*59T>G | ENSP00000493044.1:n.*59T>G | |
| ENST00000641882.1:c.*59T>G | ENSP00000493301.1:n.*59T>G | |
| ENST00000641928.1:c.*127T>G | ENSP00000493418.1:n.*127T>G | |
| ENST00000641949.1:c.554-9951T>G | ENSP00000492891.1:n.554-9951T>G | |
| ENST00000642012.1:n.758T>G | ||
| ENST00000642034.1:c.780T>G | ENSP00000493285.1:p.Tyr260Ter | |
| ENST00000642042.1:c.894T>G | ENSP00000493260.1:p.Tyr298Ter | |
| ENST00000642078.1:c.*59T>G | ENSP00000492885.1:n.*59T>G | |
| ENST00000642121.1:n.121T>G | ||
| ENST00000296468.7:c.894T>G | ENSP00000296468.3:p.Tyr298Ter | |
| ENST00000505284.5:n.789T>G | ||
| ENST00000509826.1:c.*127T>G | ENSP00000421176.1:n.*127T>G | |
| ENST00000513559.5:c.759T>G | ENSP00000425000.1:p.Tyr253Ter | |
| ENST00000515130.5:n.1340T>G | ||
| NM_152778.2:c.894T>G | NP_689991.1:p.Tyr298Ter | |
| XM_005262893.1:c.894T>G | XP_005262950.1:p.Tyr298Ter | |
| XM_005262896.1:c.747T>G | XP_005262953.1:p.Tyr249Ter | |
| XM_005262897.1:c.693T>G | XP_005262954.1:p.Tyr231Ter | |
| XM_005262898.2:c.894T>G | XP_005262955.1:p.Tyr298Ter | |
| XM_005262900.2:c.*59T>G | XP_005262957.1:n.*59T>G | |
| XM_011531830.1:c.780T>G | XP_011530132.1:p.Tyr260Ter | |
| XM_011531831.1:c.579T>G | XP_011530133.1:p.Tyr193Ter | |
| XM_011531832.1:c.780T>G | XP_011530134.1:p.Tyr260Ter | |
| XR_938717.1:n.971T>G | ||
| NM_001363520.1:c.693T>G | NP_001350449.1:p.Tyr231Ter | |
| NM_001363521.1:c.579T>G | NP_001350450.1:p.Tyr193Ter | |
| XM_005262898.3:c.894T>G | XP_005262955.1:p.Tyr298Ter | |
| XM_017007989.1:c.693T>G | XP_016863478.1:p.Tyr231Ter | |
| XM_024453981.1:c.759T>G | XP_024309749.1:p.Tyr253Ter | |
| XM_024453982.1:c.645T>G | XP_024309750.1:p.Tyr215Ter | |
| XM_024453983.1:c.444T>G | XP_024309751.1:p.Tyr148Ter | |
| XR_001741194.1:n.971T>G | ||
| XR_001741195.1:n.857T>G | ||
| XR_001741196.1:n.770T>G | ||
| XR_001741197.1:n.826T>G | ||
| XR_001741198.2:n.826T>G | ||
| XR_001741199.1:n.826T>G | ||
| XR_938717.2:n.971T>G | ||
| NM_001363520.2:c.693T>G | NP_001350449.1:p.Tyr231Ter | |
| NM_001363521.2:c.579T>G | NP_001350450.1:p.Tyr193Ter | |
| NM_001371590.1:c.759T>G | NP_001358519.1:p.Tyr253Ter | |
| NM_001371591.1:c.894T>G | NP_001358520.1:p.Tyr298Ter | |
| NM_001371592.1:c.900T>G | NP_001358521.1:p.Tyr300Ter | |
| NM_001371593.1:c.780T>G | NP_001358522.1:p.Tyr260Ter | |
| NM_001371594.1:c.747T>G | NP_001358523.1:p.Tyr249Ter | |
| NM_001371595.1:c.612T>G | NP_001358524.1:p.Tyr204Ter | |
| NM_001371596.2:c.894T>G MANE Select | NP_001358525.1:p.Tyr298Ter | |
| NM_152778.3:c.894T>G | NP_689991.1:p.Tyr298Ter | |
| NM_152778.4:c.894T>G | NP_689991.1:p.Tyr298Ter |