HGVS | Genome Assembly |
---|---|
NC_000016.10:g.2289459C>T , CM000678.2:g.2289459C>T | GRCh38 |
NC_000016.9:g.2339460C>T , CM000678.1:g.2339460C>T | GRCh37 |
NC_000016.8:g.2279461C>T | NCBI36 |
NG_011790.1:g.56288G>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000301732.10:c.2675G>A MANE Select | ENSP00000301732.5:p.Arg892His | |
ENST00000301732.9:c.2675G>A | ENSP00000301732.5:p.Arg892His | |
ENST00000382381.7:c.2501G>A | ENSP00000371818.3:p.Arg834His | |
ENST00000563623.5:n.3238G>A | ||
NM_001089.2:c.2675G>A | NP_001080.2:p.Arg892His | |
NM_001089.3:c.2675G>A MANE Select | NP_001080.2:p.Arg892His |