HGVS | Genome Assembly |
---|---|
NC_000019.10:g.855603G= , CM000681.2:g.855603G= | GRCh38 |
NC_000019.9:g.855603G= , CM000681.1:g.855603G= | GRCh37 |
NC_000019.8:g.806603G= | NCBI36 |
NG_007274.1:g.939G= , LRG_46:g.939G= | |
NG_009627.1:g.8313G= , LRG_57:g.8313G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263621.2:c.406G= MANE Select | ENSP00000263621.1:p.Ala136= | |
ENST00000263621.1:c.406G= | ENSP00000263621.1:p.Ala136= | |
ENST00000590230.5:c.406G= | ENSP00000466090.1:p.Ala136= | |
NM_001972.2:c.406G= , LRG_57t1:c.406G= | NP_001963.1:p.Ala136= | |
XM_011527775.1:c.406G= | XP_011526077.1:p.Ala136= | |
XM_011527776.1:c.406G= | XP_011526078.1:p.Ala136= | |
NM_001972.3:c.406G= | NP_001963.1:p.Ala136= | |
NM_001972.4:c.406G= MANE Select | NP_001963.1:p.Ala136= |