Linked Data
ClinVar Variation Id:
2951180
ClinVar RCV Id:
RCV003802442
dbSNP Id:
rs964109390
gnomAD v2:
17-7906539-C-T
gnomAD v3:
17-8003221-C-T
gnomAD v4:
17-8003221-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8003221C>T , CM000679.2:g.8003221C>T | GRCh38 |
| NC_000017.10:g.7906539C>T , CM000679.1:g.7906539C>T | GRCh37 |
| NC_000017.9:g.7847264C>T | NCBI36 |
| NG_009092.1:g.5552C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000254854.5:c.174C>T MANE Select | ENSP00000254854.4:p.Val58= | |
| ENST00000254854.4:c.174C>T | ENSP00000254854.4:p.Val58= | |
| NM_000180.3:c.174C>T | NP_000171.1:p.Val58= | |
| XM_011523816.1:c.174C>T | XP_011522118.1:p.Val58= | |
| NM_000180.4:c.174C>T MANE Select | NP_000171.1:p.Val58= |