Linked Data
ClinVar Variation Id:
2257521
ClinVar RCV Id:
RCV002792444
dbSNP Id:
rs976018810
gnomAD v4:
3-138945786-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.138945786C>T , CM000665.2:g.138945786C>T | GRCh38 |
| NC_000003.11:g.138664628C>T , CM000665.1:g.138664628C>T | GRCh37 |
| NC_000003.10:g.140147318C>T | NCBI36 |
| NG_012454.1:g.6355G>A | |
| NG_029796.1:g.3553C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000648323.1:c.937G>A MANE Select | ENSP00000497217.1:p.Gly313Arg | |
| ENST00000330315.3:c.937G>A | ENSP00000333188.3:p.Gly313Arg | |
| NM_023067.3:c.937G>A | NP_075555.1:p.Gly313Arg | |
| NM_023067.4:c.937G>A MANE Select | NP_075555.1:p.Gly313Arg |