HGVS | Genome Assembly |
---|---|
NC_000011.10:g.112228658G= , CM000673.2:g.112228658G= | GRCh38 |
NC_000011.9:g.112099381G= , CM000673.1:g.112099381G= | GRCh37 |
NC_000011.8:g.111604591G= | NCBI36 |
NG_008743.1:g.7294G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000280362.8:c.148G= MANE Select | ENSP00000280362.3:p.Gly50= | |
ENST00000280362.7:c.148G= | ENSP00000280362.3:p.Gly50= | |
ENST00000524931.1:c.-57G= | ENSP00000434688.1:n.-57G= | |
ENST00000525645.1:n.223G= | ||
ENST00000525803.1:c.148G= | ENSP00000431750.1:p.Gly50= | |
ENST00000528679.5:c.148G= | ENSP00000435895.1:p.Gly50= | |
ENST00000531673.5:c.148G= | ENSP00000433469.1:p.Gly50= | |
NM_000317.2:c.148G= | NP_000308.1:p.Gly50= | |
NM_000317.3:c.148G= MANE Select | NP_000308.1:p.Gly50= |