HGVS | Genome Assembly |
---|---|
NC_000010.11:g.80275180C>G , CM000672.2:g.80275180C>G | GRCh38 |
NC_000010.10:g.82034936C>G , CM000672.1:g.82034936C>G | GRCh37 |
NC_000010.9:g.82024916C>G | NCBI36 |
NG_008083.1:g.19499G>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000372213.8:c.788G>C MANE Select | ENSP00000361287.3:p.Gly263Ala | |
ENST00000372213.7:c.788G>C | ENSP00000361287.3:p.Gly263Ala | |
ENST00000480845.1:n.20G>C | ||
ENST00000485270.5:n.300G>C | ||
NM_000429.2:c.788G>C | NP_000420.1:p.Gly263Ala | |
XM_005269842.3:c.788G>C | XP_005269899.1:p.Gly263Ala | |
XM_005269843.3:c.665G>C | XP_005269900.1:p.Gly222Ala | |
NM_000429.3:c.788G>C MANE Select | NP_000420.1:p.Gly263Ala |