HGVS | Genome Assembly |
---|---|
NC_000007.14:g.21748707A= , CM000669.2:g.21748707A= | GRCh38 |
NC_000007.13:g.21788325A= , CM000669.1:g.21788325A= | GRCh37 |
NC_000007.12:g.21754850A= | NCBI36 |
NG_012886.2:g.210493A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000409508.8:c.8638A= MANE Select | ENSP00000475939.1:p.Thr2880= | |
ENST00000328843.10:c.8659A= | ENSP00000330671.7:p.Thr2887= | |
ENST00000409508.7:c.8638A= | ENSP00000475939.1:p.Thr2880= | |
ENST00000620169.4:c.8659A= | ENSP00000481693.1:p.Thr2887= | |
NM_001277115.1:c.8638A= | NP_001264044.1:p.Thr2880= | |
NM_001277115.2:c.8638A= MANE Select | NP_001264044.1:p.Thr2880= |