HGVS | Genome Assembly |
---|---|
NC_000005.10:g.159320608A>T , CM000667.2:g.159320608A>T | GRCh38 |
NC_000005.9:g.158747616A>T , CM000667.1:g.158747616A>T | GRCh37 |
NC_000005.8:g.158680194A>T | NCBI36 |
NG_009618.1:g.14866T>A , LRG_71:g.14866T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000696750.1:c.-148-88T>A | ENSP00000512849.1:n.-148-88T>A | |
ENST00000696751.1:c.365-88T>A | ENSP00000512850.1:n.365-88T>A | |
ENST00000231228.3:c.483-88T>A MANE Select | ENSP00000231228.2:n.483-88T>A | |
ENST00000231228.2:c.483-88T>A | ENSP00000231228.2:n.483-88T>A | |
NM_002187.2:c.483-88T>A , LRG_71t1:c.483-88T>A | NP_002178.2:n.483-88T>A | |
XR_001742945.1:n.147+12A>T | ||
NM_002187.3:c.483-88T>A MANE Select | NP_002178.2:n.483-88T>A |