HGVS | Genome Assembly |
---|---|
NC_000012.12:g.4912604C= , CM000674.2:g.4912604C= | GRCh38 |
NC_000012.11:g.5021770C= , CM000674.1:g.5021770C= | GRCh37 |
NC_000012.10:g.4892031C= | NCBI36 |
NG_011815.1:g.7698C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382545.5:c.1226C= MANE Select | ENSP00000371985.3:p.Ser409= | |
ENST00000543874.3:n.105+2132C= | ||
ENST00000639306.1:c.1064C= | ENSP00000492506.1:p.Ser355= | |
ENST00000639680.1:c.76+338C= | ||
ENST00000382545.3:c.1226C= | ENSP00000371985.3:p.Ser409= | |
ENST00000541095.1:n.105+2132C= | ||
ENST00000543874.2:n.96+2132C= | ||
NM_000217.2:c.1226C= | NP_000208.2:p.Ser409= | |
NM_000217.3:c.1226C= MANE Select | NP_000208.2:p.Ser409= |