HGVS | Genome Assembly |
---|---|
NC_000023.11:g.106033584A>T , CM000685.2:g.106033584A>T | GRCh38 |
NC_000023.10:g.105277575A>T , CM000685.1:g.105277575A>T | GRCh37 |
NC_000023.9:g.105164231A>T | NCBI36 |
NG_021252.1:g.10144T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000372563.2:c.1164T>A MANE Select | ENSP00000361644.1:p.Asp388Glu | |
ENST00000327674.8:c.1164T>A | ENSP00000329374.4:p.Asp388Glu | |
ENST00000372563.1:c.1164T>A | ENSP00000361644.1:p.Asp388Glu | |
NM_000354.5:c.1164T>A | NP_000345.2:p.Asp388Glu | |
XM_006724683.1:c.1194T>A | XP_006724746.1:p.Asp398Glu | |
XM_005262180.4:c.*109T>A | XP_005262237.1:n.*109T>A | |
XM_006724683.2:c.1194T>A | XP_006724746.1:p.Asp398Glu | |
NM_000354.6:c.1164T>A MANE Select | NP_000345.2:p.Asp388Glu |