HGVS | Genome Assembly |
---|---|
NC_000007.14:g.2830351T>A , CM000669.2:g.2830351T>A | GRCh38 |
NC_000007.13:g.2869985T>A , CM000669.1:g.2869985T>A | GRCh37 |
NC_000007.12:g.2836511T>A | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000275364.8:c.309+13502A>T MANE Select | ENSP00000275364.3:n.309+13502A>T | |
ENST00000275364.7:c.309+13502A>T | ENSP00000275364.3:n.309+13502A>T | |
NM_001293092.1:c.309+13502A>T | NP_001280021.1:n.309+13502A>T | |
NM_007353.2:c.309+13502A>T | NP_031379.2:n.309+13502A>T | |
XM_011515288.1:c.19-35208A>T | XP_011513590.1:n.19-35208A>T | |
XM_011515288.3:c.19-35208A>T | XP_011513590.1:n.19-35208A>T | |
NM_007353.3:c.309+13502A>T MANE Select | NP_031379.2:n.309+13502A>T | |
NM_001293092.2:c.309+13502A>T | NP_001280021.1:n.309+13502A>T |