HGVS | Genome Assembly |
---|---|
NC_000020.11:g.23637665G>T , CM000682.2:g.23637665G>T | GRCh38 |
NC_000020.10:g.23618302G>T , CM000682.1:g.23618302G>T | GRCh37 |
NC_000020.9:g.23566302G>T | NCBI36 |
NG_012887.2:g.5273C>A | |
NG_012887.3:g.5273C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000376925.8:c.198C>A MANE Select | ENSP00000366124.3:p.Asp66Glu | |
ENST00000376925.7:c.198C>A | ENSP00000366124.3:p.Asp66Glu | |
ENST00000398409.1:c.198C>A | ENSP00000381446.1:p.Asp66Glu | |
ENST00000398411.5:c.198C>A | ENSP00000381448.1:p.Asp66Glu | |
NM_000099.3:c.198C>A | NP_000090.1:p.Asp66Glu | |
NM_001288614.1:c.198C>A | NP_001275543.1:p.Asp66Glu | |
NM_000099.4:c.198C>A MANE Select | NP_000090.1:p.Asp66Glu | |
NM_001288614.2:c.198C>A | NP_001275543.1:p.Asp66Glu |