HGVS | Genome Assembly |
---|---|
NC_000012.12:g.48981549T>G , CM000674.2:g.48981549T>G | GRCh38 |
NC_000012.11:g.49375332T>G , CM000674.1:g.49375332T>G | GRCh37 |
NC_000012.10:g.47661599T>G | NCBI36 |
NG_033141.1:g.8097T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000293549.4:c.1022T>G MANE Select | ENSP00000293549.3:p.Val341Gly | |
ENST00000293549.3:c.1022T>G | ENSP00000293549.3:p.Val341Gly | |
ENST00000613114.4:c.989T>G | ENSP00000481240.1:p.Val330Gly | |
NM_005430.3:c.1022T>G | NP_005421.1:p.Val341Gly | |
NM_005430.4:c.1022T>G MANE Select | NP_005421.1:p.Val341Gly |