Linked Data
ClinVar Variation Id:
241721
dbSNP Id:
rs375349195
ExAC:
3:128205693 G / A
gnomAD v2:
3-128205693-G-A
gnomAD v4:
3-128486850-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.128486850G>A , CM000665.2:g.128486850G>A | GRCh38 |
| NC_000003.11:g.128205693G>A , CM000665.1:g.128205693G>A | GRCh37 |
| NC_000003.10:g.129688383G>A | NCBI36 |
| NG_029334.1:g.11338C>T , LRG_295:g.11338C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000487848.6:c.182C>T MANE Plus Clinical | ENSP00000417074.1:p.Ala61Val | |
| ENST00000696466.1:c.464C>T | ENSP00000512647.1:p.Ala155Val | |
| ENST00000696652.1:c.182C>T | ENSP00000512781.1:p.Ala61Val | |
| ENST00000696653.1:c.182C>T | ENSP00000512782.1:p.Ala61Val | |
| ENST00000696654.1:c.182C>T | ENSP00000512783.1:p.Ala61Val | |
| ENST00000696661.1:c.182C>T | ENSP00000512787.1:p.Ala61Val | |
| ENST00000341105.7:c.182C>T MANE Select | ENSP00000345681.2:p.Ala61Val | |
| ENST00000341105.6:c.182C>T | ENSP00000345681.2:p.Ala61Val | |
| ENST00000430265.6:c.182C>T | ENSP00000400259.2:p.Ala61Val | |
| ENST00000487848.5:c.182C>T | ENSP00000417074.1:p.Ala61Val | |
| ENST00000492608.1:c.182C>T | ENSP00000418132.1:p.Ala61Val | |
| NM_001145661.1:c.182C>T , LRG_295t1:c.182C>T | NP_001139133.1:p.Ala61Val | |
| NM_001145662.1:c.182C>T | NP_001139134.1:p.Ala61Val | |
| NM_032638.4:c.182C>T , LRG_295t2:c.182C>T | NP_116027.2:p.Ala61Val | |
| NM_001145661.2:c.182C>T MANE Plus Clinical | NP_001139133.1:p.Ala61Val | |
| NM_032638.5:c.182C>T MANE Select | NP_116027.2:p.Ala61Val |