HGVS | Genome Assembly |
---|---|
NC_000003.12:g.138945742T>A , CM000665.2:g.138945742T>A | GRCh38 |
NC_000003.11:g.138664584T>A , CM000665.1:g.138664584T>A | GRCh37 |
NC_000003.10:g.140147274T>A | NCBI36 |
NG_012454.1:g.6399A>T | |
NG_029796.1:g.3509T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000648323.1:c.981A>T MANE Select | ENSP00000497217.1:p.Pro327= | |
ENST00000330315.3:c.981A>T | ENSP00000333188.3:p.Pro327= | |
NM_023067.3:c.981A>T | NP_075555.1:p.Pro327= | |
NM_023067.4:c.981A>T MANE Select | NP_075555.1:p.Pro327= |