Linked Data
ClinVar Variation Id:
347542
dbSNP Id:
rs747197852
ExAC:
4:128842922 C / G
gnomAD v2:
4-128842922-C-G
gnomAD v3:
4-127921767-C-G
gnomAD v4:
4-127921767-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.127921767C>G , CM000666.2:g.127921767C>G | GRCh38 |
| NC_000004.11:g.128842922C>G , CM000666.1:g.128842922C>G | GRCh37 |
| NC_000004.10:g.129062372C>G | NCBI36 |
| NG_008657.1:g.49218G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296468.8:c.1107G>C | ENSP00000296468.3:p.Leu369Phe | |
| ENST00000509826.2:c.*428G>C | ENSP00000421176.2:n.*428G>C | |
| ENST00000513559.6:c.825G>C | ENSP00000425000.2:p.Leu275Phe | |
| ENST00000515130.6:c.868G>C | ENSP00000493056.1:p.Ala290Pro | |
| ENST00000641025.1:c.1003G>C | ENSP00000493346.1:p.Ala335Pro | |
| ENST00000641092.1:c.802G>C | ENSP00000493392.1:p.Ala268Pro | |
| ENST00000641133.1:c.*421G>C | ENSP00000493192.1:n.*421G>C | |
| ENST00000641146.1:n.973G>C | ||
| ENST00000641147.1:c.657G>C | ENSP00000493133.1:p.Leu219Phe | |
| ENST00000641178.1:c.972G>C | ENSP00000492989.1:p.Leu324Phe | |
| ENST00000641186.1:c.993G>C | ENSP00000493347.1:p.Leu331Phe | |
| ENST00000641228.1:c.802G>C | ENSP00000493194.1:p.Ala268Pro | |
| ENST00000641332.1:c.*168G>C | ENSP00000493397.1:n.*168G>C | |
| ENST00000641340.1:c.*236G>C | ENSP00000493191.1:n.*236G>C | |
| ENST00000641388.1:n.354G>C | ||
| ENST00000641393.1:c.657G>C | ENSP00000493197.1:p.Leu219Phe | |
| ENST00000641397.1:c.688G>C | ENSP00000493406.1:p.Ala230Pro | |
| ENST00000641413.1:c.32G>C | ||
| ENST00000641434.1:c.1107G>C | ENSP00000493279.1:p.Leu369Phe | |
| ENST00000641464.1:c.*340G>C | ENSP00000493438.1:n.*340G>C | |
| ENST00000641482.1:c.1003G>C | ENSP00000493277.1:p.Ala335Pro | |
| ENST00000641508.1:c.*340G>C | ENSP00000493209.1:n.*340G>C | |
| ENST00000641509.1:c.792G>C | ENSP00000493459.1:p.Leu264Phe | |
| ENST00000641590.1:c.889G>C | ENSP00000493132.1:p.Ala297Pro | |
| ENST00000641658.1:c.*272G>C | ENSP00000492987.1:n.*272G>C | |
| ENST00000641686.2:c.1107G>C MANE Select | ENSP00000493218.2:p.Leu369Phe | |
| ENST00000641690.1:c.906G>C | ENSP00000492966.1:p.Leu302Phe | |
| ENST00000641742.1:c.*272G>C | ENSP00000493315.1:n.*272G>C | |
| ENST00000641748.1:c.1107G>C | ENSP00000493330.1:p.Leu369Phe | |
| ENST00000641753.1:c.934G>C | ||
| ENST00000641774.1:c.*359G>C | ENSP00000492960.1:n.*359G>C | |
| ENST00000641830.1:c.339G>C | ||
| ENST00000641843.1:c.*168G>C | ENSP00000493174.1:n.*168G>C | |
| ENST00000641869.1:c.308G>C | ||
| ENST00000641870.1:c.*168G>C | ENSP00000493044.1:n.*168G>C | |
| ENST00000641882.1:c.*272G>C | ENSP00000493301.1:n.*272G>C | |
| ENST00000641928.1:c.*236G>C | ENSP00000493418.1:n.*236G>C | |
| ENST00000641949.1:c.554-931G>C | ENSP00000492891.1:n.554-931G>C | |
| ENST00000642012.1:n.971G>C | ||
| ENST00000642034.1:c.889G>C | ENSP00000493285.1:p.Ala297Pro | |
| ENST00000642042.1:c.1107G>C | ENSP00000493260.1:p.Leu369Phe | |
| ENST00000642078.1:c.*168G>C | ENSP00000492885.1:n.*168G>C | |
| ENST00000296468.7:c.1107G>C | ENSP00000296468.3:p.Leu369Phe | |
| ENST00000504126.1:n.135G>C | ||
| ENST00000505284.5:n.898G>C | ||
| ENST00000513559.5:c.972G>C | ENSP00000425000.1:p.Leu324Phe | |
| ENST00000515130.5:n.1449G>C | ||
| NM_152778.2:c.1107G>C | NP_689991.1:p.Leu369Phe | |
| XM_005262893.1:c.1107G>C | XP_005262950.1:p.Leu369Phe | |
| XM_005262896.1:c.960G>C | XP_005262953.1:p.Leu320Phe | |
| XM_005262897.1:c.906G>C | XP_005262954.1:p.Leu302Phe | |
| XM_005262898.2:c.1003G>C | XP_005262955.1:p.Ala335Pro | |
| XM_011531830.1:c.993G>C | XP_011530132.1:p.Leu331Phe | |
| XM_011531831.1:c.792G>C | XP_011530133.1:p.Leu264Phe | |
| XM_011531832.1:c.889G>C | XP_011530134.1:p.Ala297Pro | |
| XR_938717.1:n.1184G>C | ||
| NM_001363520.1:c.906G>C | NP_001350449.1:p.Leu302Phe | |
| NM_001363521.1:c.792G>C | NP_001350450.1:p.Leu264Phe | |
| XM_005262898.3:c.1003G>C | XP_005262955.1:p.Ala335Pro | |
| XM_017007989.1:c.802G>C | XP_016863478.1:p.Ala268Pro | |
| XM_024453981.1:c.972G>C | XP_024309749.1:p.Leu324Phe | |
| XM_024453982.1:c.858G>C | XP_024309750.1:p.Leu286Phe | |
| XM_024453983.1:c.657G>C | XP_024309751.1:p.Leu219Phe | |
| XR_001741194.1:n.1080G>C | ||
| XR_001741195.1:n.966G>C | ||
| XR_001741196.1:n.879G>C | ||
| XR_001741197.1:n.1039G>C | ||
| XR_001741198.2:n.935G>C | ||
| XR_001741199.1:n.935G>C | ||
| XR_938717.2:n.1184G>C | ||
| NM_001363520.2:c.906G>C | NP_001350449.1:p.Leu302Phe | |
| NM_001363521.2:c.792G>C | NP_001350450.1:p.Leu264Phe | |
| NM_001371590.1:c.972G>C | NP_001358519.1:p.Leu324Phe | |
| NM_001371591.1:c.1107G>C | NP_001358520.1:p.Leu369Phe | |
| NM_001371592.1:c.1113G>C | NP_001358521.1:p.Leu371Phe | |
| NM_001371593.1:c.993G>C | NP_001358522.1:p.Leu331Phe | |
| NM_001371594.1:c.960G>C | NP_001358523.1:p.Leu320Phe | |
| NM_001371595.1:c.825G>C | NP_001358524.1:p.Leu275Phe | |
| NM_001371596.2:c.1107G>C MANE Select | NP_001358525.1:p.Leu369Phe | |
| NM_152778.3:c.1107G>C | NP_689991.1:p.Leu369Phe | |
| NM_152778.4:c.1107G>C | NP_689991.1:p.Leu369Phe |