HGVS | Genome Assembly |
---|---|
NC_000003.12:g.138945966C>T , CM000665.2:g.138945966C>T | GRCh38 |
NC_000003.11:g.138664808C>T , CM000665.1:g.138664808C>T | GRCh37 |
NC_000003.10:g.140147498C>T | NCBI36 |
NG_012454.1:g.6175G>A | |
NG_029796.1:g.3733C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000648323.1:c.757G>A MANE Select | ENSP00000497217.1:p.Ala253Thr | |
ENST00000330315.3:c.757G>A | ENSP00000333188.3:p.Ala253Thr | |
NM_023067.3:c.757G>A | NP_075555.1:p.Ala253Thr | |
NM_023067.4:c.757G>A MANE Select | NP_075555.1:p.Ala253Thr |