HGVS | Genome Assembly |
---|---|
NC_000012.12:g.113463332C>T , CM000674.2:g.113463332C>T | GRCh38 |
NC_000012.11:g.113901137C>T , CM000674.1:g.113901137C>T | GRCh37 |
NC_000012.10:g.112385520C>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261731.4:c.1067G>A MANE Select | ENSP00000261731.2:p.Gly356Asp | |
ENST00000261731.3:c.1067G>A | ENSP00000261731.2:p.Gly356Asp | |
NM_022363.2:c.1067G>A | NP_071758.1:p.Gly356Asp | |
NM_022363.3:c.1067G>A MANE Select | NP_071758.1:p.Gly356Asp |