HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154997073C>A , CM000685.2:g.154997073C>A | GRCh38 |
NC_000023.10:g.154225348C>A , CM000685.1:g.154225348C>A | GRCh37 |
NC_000023.9:g.153878542C>A | NCBI36 |
NG_011403.1:g.30651G>T | |
NG_011403.2:g.30651G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360256.9:c.288G>T MANE Select | ENSP00000353393.4:p.Gln96His | |
ENST00000647125.1:c.*74G>T | ENSP00000496062.1:n.*74G>T | |
ENST00000360256.8:c.288G>T | ENSP00000353393.4:p.Gln96His | |
ENST00000423959.5:c.183G>T | ENSP00000409446.1:p.Gln61His | |
ENST00000453950.1:c.270G>T | ENSP00000389153.1:p.Gln90His | |
NM_000132.3:c.288G>T | NP_000123.1:p.Gln96His | |
XM_011531126.1:c.183G>T | XP_011529428.1:p.Gln61His | |
NM_000132.4:c.288G>T MANE Select | NP_000123.1:p.Gln96His |