HGVS | Genome Assembly |
---|---|
NC_000008.11:g.16992778C>A , CM000670.2:g.16992778C>A | GRCh38 |
NC_000008.10:g.16850287C>A , CM000670.1:g.16850287C>A | GRCh37 |
NC_000008.9:g.16894658C>A | NCBI36 |
NG_015978.1:g.14388G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000180166.6:c.*294G>T MANE Select | ENSP00000180166.5:n.*294G>T | |
ENST00000180166.5:c.*294G>T | ENSP00000180166.5:n.*294G>T | |
NM_019851.3:c.*294G>T MANE Select | NP_062825.1:n.*294G>T |