HGVS | Genome Assembly |
---|---|
NC_000019.10:g.18786117T>G , CM000681.2:g.18786117T>G | GRCh38 |
NC_000019.9:g.18896927T>G , CM000681.1:g.18896927T>G | GRCh37 |
NC_000019.8:g.18757927T>G | NCBI36 |
NG_007070.1:g.10188A>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000222271.7:c.1337A>C MANE Select | ENSP00000222271.2:p.Asp446Ala | |
ENST00000222271.6:c.1337A>C | ENSP00000222271.2:p.Asp446Ala | |
ENST00000425807.1:c.1178A>C | ENSP00000403792.1:p.Asp393Ala | |
ENST00000542601.6:c.1238A>C | ENSP00000439156.2:p.Asp413Ala | |
NM_000095.2:c.1337A>C | NP_000086.2:p.Asp446Ala | |
NM_000095.3:c.1337A>C MANE Select | NP_000086.2:p.Asp446Ala |