HGVS | Genome Assembly |
---|---|
NC_000001.11:g.17024021G= , CM000663.2:g.17024021G= | GRCh38 |
NC_000001.10:g.17350516G= , CM000663.1:g.17350516G= | GRCh37 |
NC_000001.9:g.17223103G= | NCBI36 |
NG_012340.1:g.35150C= , LRG_316:g.35150C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000463045.3:c.423C= | ENSP00000481376.2:p.Ser141= | |
ENST00000491274.6:c.552C= | ENSP00000480482.2:p.Ser184= | |
ENST00000375499.8:c.594C= MANE Select | ENSP00000364649.3:p.Ser198= | |
ENST00000375499.7:c.594C= | ENSP00000364649.3:p.Ser198= | |
ENST00000485515.5:n.528C= | ||
ENST00000491274.5:c.552C= | ENSP00000480482.1:p.Ser184= | |
NM_003000.2:c.594C= , LRG_316t1:c.594C= | NP_002991.2:p.Ser198= | |
NM_003000.3:c.594C= MANE Select | NP_002991.2:p.Ser198= |