HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31622884A>G , CM000668.2:g.31622884A>G | GRCh38 |
NC_000006.11:g.31590661A>G , CM000668.1:g.31590661A>G | GRCh37 |
NC_000006.10:g.31698640A>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000376033.3:c.95A>G MANE Select | ENSP00000365201.2:p.Glu32Gly | |
ENST00000376007.8:c.95A>G | ENSP00000365175.4:p.Glu32Gly | |
ENST00000376033.2:c.95A>G | ENSP00000365201.2:p.Glu32Gly | |
ENST00000469577.5:n.136-1377A>G | ||
NM_004638.3:c.95A>G | NP_004629.3:p.Glu32Gly | |
NM_080686.2:c.95A>G | NP_542417.2:p.Glu32Gly | |
XM_011514890.1:c.95A>G | XP_011513192.1:p.Glu32Gly | |
XM_017011274.1:c.95A>G | XP_016866763.1:p.Glu32Gly | |
NM_004638.4:c.95A>G MANE Select | NP_004629.3:p.Glu32Gly | |
NM_080686.3:c.95A>G | NP_542417.2:p.Glu32Gly |