Linked Data
ClinVar Variation Id:
217598
dbSNP Id:
rs863225170
gnomAD v2:
4-15570969-T-C
gnomAD v3:
4-15569346-T-C
gnomAD v4:
4-15569346-T-C
PubMed:
PMID:26092869
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.15569346T>C , CM000666.2:g.15569346T>C | GRCh38 |
| NC_000004.11:g.15570969T>C , CM000666.1:g.15570969T>C | GRCh37 |
| NC_000004.10:g.15180067T>C | NCBI36 |
| NG_013035.1:g.104481T>C , LRG_697:g.104481T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000389652.11:c.3467T>C | ENSP00000374303.8:p.Val1156Ala | |
| ENST00000424120.6:c.3452T>C MANE Select | ENSP00000403465.1:p.Val1151Ala | |
| ENST00000503292.6:c.3452T>C | ENSP00000421809.1:p.Val1151Ala | |
| ENST00000506643.5:c.3305T>C | ENSP00000422931.2:p.Val1102Ala | |
| ENST00000634028.2:c.3305T>C | ENSP00000488669.2:p.Val1102Ala | |
| ENST00000650860.2:c.*458T>C | ENSP00000498775.1:n.*458T>C | |
| ENST00000674945.1:c.3305T>C | ENSP00000502333.1:p.Val1102Ala | |
| ENST00000675619.1:n.4263T>C | ||
| ENST00000675768.1:n.672T>C | ||
| ENST00000676337.1:c.*458T>C | ENSP00000501728.1:n.*458T>C | |
| ENST00000680586.1:n.4111T>C | ||
| ENST00000389652.9:c.2929T>C | ||
| ENST00000424120.5:c.3452T>C | ENSP00000403465.1:p.Val1151Ala | |
| ENST00000503292.5:c.3452T>C | ENSP00000421809.1:p.Val1151Ala | |
| ENST00000506643.4:c.1780T>C | ||
| ENST00000634028.1:c.3435T>C | ENSP00000488669.1:n.3435T>C | |
| NM_001080522.2:c.3452T>C , LRG_697t1:c.3452T>C | NP_001073991.2:p.Val1151Ala | |
| XM_005248177.1:c.3452T>C | XP_005248234.1:p.Val1151Ala | |
| XM_011513869.1:c.3452T>C | XP_011512171.1:p.Val1151Ala | |
| XM_011513870.1:c.3452T>C | XP_011512172.1:p.Val1151Ala | |
| XM_011513871.1:c.3305T>C | XP_011512173.1:p.Val1102Ala | |
| XM_017008482.1:c.3305T>C | XP_016863971.1:p.Val1102Ala | |
| XR_001741296.1:n.3697T>C | ||
| NM_001378615.1:c.3452T>C MANE Select | NP_001365544.1:p.Val1151Ala | |
| NM_001378617.1:c.3305T>C | NP_001365546.1:p.Val1102Ala |