HGVS | Genome Assembly |
---|---|
NC_000017.11:g.30224973T>A , CM000679.2:g.30224973T>A | GRCh38 |
NC_000017.10:g.28551991T>A , CM000679.1:g.28551991T>A | GRCh37 |
NC_000017.9:g.25576117T>A | NCBI36 |
NG_011747.2:g.15964A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000650711.1:c.-220-2058A>T MANE Select | ENSP00000498537.1:n.-220-2058A>T | |
ENST00000261707.7:c.-220-2058A>T | ENSP00000261707.3:n.-220-2058A>T | |
ENST00000394821.2:c.-220-2058A>T | ENSP00000378298.2:n.-220-2058A>T | |
ENST00000401766.6:c.-123-2892A>T | ENSP00000385822.2:n.-123-2892A>T | |
NM_001045.5:c.-220-2058A>T | NP_001036.1:n.-220-2058A>T | |
NM_001045.6:c.-220-2058A>T MANE Select | NP_001036.1:n.-220-2058A>T |