Linked Data
ClinVar Variation Id:
335691
dbSNP Id:
rs74716434
ExAC:
2:29430136 G / A
gnomAD v2:
2-29430136-G-A
gnomAD v3:
2-29207270-G-A
gnomAD v4:
2-29207270-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.29207270G>A , CM000664.2:g.29207270G>A | GRCh38 |
| NC_000002.11:g.29430136G>A , CM000664.1:g.29430136G>A | GRCh37 |
| NC_000002.10:g.29283640G>A | NCBI36 |
| NG_009445.1:g.719297C>T , LRG_488:g.719297C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000389048.8:c.3839C>T MANE Select | ENSP00000373700.3:p.Ala1280Val | |
| ENST00000431873.6:c.1066C>T | ||
| ENST00000638605.1:n.716C>T | ||
| ENST00000642122.1:c.635C>T | ENSP00000493203.1:p.Ala212Val | |
| ENST00000389048.7:c.3839C>T | ENSP00000373700.3:p.Ala1280Val | |
| ENST00000431873.5:c.719C>T | ENSP00000414027.2:p.Ala240Val | |
| ENST00000618119.4:c.2708C>T | ENSP00000482733.1:p.Ala903Val | |
| NM_004304.4:c.3839C>T | NP_004295.2:p.Ala1280Val | |
| NM_001353765.1:c.635C>T | NP_001340694.1:p.Ala212Val | |
| XM_024452778.1:c.992C>T | XP_024308546.1:p.Ala331Val | |
| XM_024452779.1:c.635C>T | XP_024308547.1:p.Ala212Val | |
| NM_004304.5:c.3839C>T MANE Select | NP_004295.2:p.Ala1280Val | |
| NM_001353765.2:c.635C>T | NP_001340694.1:p.Ala212Val |