HGVS | Genome Assembly |
---|---|
NC_000001.11:g.109264516C= , CM000663.2:g.109264516C= | GRCh38 |
NC_000001.10:g.109807138C= , CM000663.1:g.109807138C= | GRCh37 |
NC_000001.9:g.109608661C= | NCBI36 |
NG_052669.1:g.19812C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000271332.4:c.5352C= MANE Select | ENSP00000271332.3:p.Ser1784= | |
ENST00000271332.3:c.5352C= | ENSP00000271332.3:p.Ser1784= | |
NM_001408.2:c.5352C= | NP_001399.1:p.Ser1784= | |
XM_005270580.3:c.5352C= | XP_005270637.1:p.Ser1784= | |
NM_001408.3:c.5352C= MANE Select | NP_001399.1:p.Ser1784= |