HGVS | Genome Assembly |
---|---|
NC_000020.11:g.59024036C>G , CM000682.2:g.59024036C>G | GRCh38 |
NC_000020.10:g.57599091C>G , CM000682.1:g.57599091C>G | GRCh37 |
NC_000020.9:g.57032486C>G | NCBI36 |
NG_023424.2:g.9783C>G , LRG_581:g.9783C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000217133.2:c.609C>G MANE Select | ENSP00000217133.1:p.Asp203Glu | |
ENST00000217133.1:c.609C>G | ENSP00000217133.1:p.Asp203Glu | |
NM_030773.3:c.609C>G , LRG_581t1:c.609C>G | NP_110400.1:p.Asp203Glu | |
XM_017028085.1:c.543C>G | XP_016883574.1:p.Asp181Glu | |
NM_030773.4:c.609C>G MANE Select | NP_110400.1:p.Asp203Glu |