Linked Data
ClinVar Variation Id:
2050834
ClinVar RCV Id:
RCV002922105
dbSNP Id:
rs771472612
gnomAD v2:
21-46896293-C-T
gnomAD v4:
21-45476379-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.45476379C>T , CM000683.2:g.45476379C>T | GRCh38 |
| NC_000021.8:g.46896293C>T , CM000683.1:g.46896293C>T | GRCh37 |
| NC_000021.7:g.45720721C>T | NCBI36 |
| NG_011903.1:g.76197C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355480.10:c.1367C>T | ENSP00000347665.5:p.Ala456Val | |
| ENST00000651438.1:c.827C>T MANE Select | ENSP00000498485.1:p.Ala276Val | |
| ENST00000355480.9:c.1367C>T | ENSP00000347665.5:p.Ala456Val | |
| ENST00000359759.8:c.2072C>T | ENSP00000352798.4:p.Ala691Val | |
| ENST00000400337.6:c.827C>T | ENSP00000383191.2:p.Ala276Val | |
| NM_030582.3:c.1367C>T | NP_085059.2:p.Ala456Val | |
| NM_130444.2:c.2072C>T | NP_569711.2:p.Ala691Val | |
| NM_130445.3:c.827C>T | NP_569712.2:p.Ala276Val | |
| NM_030582.4:c.1367C>T | NP_085059.2:p.Ala456Val | |
| NM_130444.3:c.2072C>T | NP_569711.2:p.Ala691Val | |
| NM_130445.4:c.827C>T | NP_569712.2:p.Ala276Val | |
| NM_001379500.1:c.827C>T MANE Select | NP_001366429.1:p.Ala276Val |