HGVS | Genome Assembly |
---|---|
NC_000001.11:g.162199399A= , CM000663.2:g.162199399A= | GRCh38 |
NC_000001.10:g.162169189A= , CM000663.1:g.162169189A= | GRCh37 |
NC_000001.9:g.160435813A= | NCBI36 |
NG_015979.1:g.134609A= | |
NG_015979.2:g.134609A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361897.10:c.177+44923A= MANE Select | ENSP00000355133.5:n.177+44923A= | |
ENST00000361897.9:c.177+44923A= | ENSP00000355133.5:n.177+44923A= | |
ENST00000430120.3:c.177+44923A= | ENSP00000396713.3:n.177+44923A= | |
ENST00000530878.5:c.177+44923A= | ENSP00000431586.1:n.177+44923A= | |
NM_001164757.1:c.177+44923A= | NP_001158229.1:n.177+44923A= | |
NM_014697.2:c.177+44923A= | NP_055512.1:n.177+44923A= | |
NM_014697.3:c.177+44923A= MANE Select | NP_055512.1:n.177+44923A= | |
NM_001164757.2:c.177+44923A= | NP_001158229.1:n.177+44923A= |