HGVS | Genome Assembly |
---|---|
NC_000003.12:g.184060213G>T , CM000665.2:g.184060213G>T | GRCh38 |
NC_000003.11:g.183778001G>T , CM000665.1:g.183778001G>T | GRCh37 |
NC_000003.10:g.185260695G>T | NCBI36 |
NG_012749.1:g.12167G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000318351.2:c.1205G>T MANE Select | ENSP00000322617.1:p.Gly402Val | |
ENST00000318351.1:c.1205G>T | ENSP00000322617.1:p.Gly402Val | |
NM_130770.2:c.1205G>T | NP_570126.2:p.Gly402Val | |
NM_130770.3:c.1205G>T MANE Select | NP_570126.2:p.Gly402Val |