HGVS | Genome Assembly |
---|---|
NC_000001.11:g.183207908A>G , CM000663.2:g.183207908A>G | GRCh38 |
NC_000001.10:g.183177043A>G , CM000663.1:g.183177043A>G | GRCh37 |
NC_000001.9:g.181443666A>G | NCBI36 |
NG_007079.2:g.26645A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264144.5:c.107A>G MANE Select | ENSP00000264144.4:p.Gln36Arg | |
ENST00000264144.4:c.107A>G | ENSP00000264144.4:p.Gln36Arg | |
ENST00000493293.5:c.107A>G | ENSP00000432063.1:p.Gln36Arg | |
NM_005562.2:c.107A>G | NP_005553.2:p.Gln36Arg | |
NM_018891.2:c.107A>G | NP_061486.2:p.Gln36Arg | |
XM_017001273.2:c.107A>G | XP_016856762.1:p.Gln36Arg | |
NM_005562.3:c.107A>G MANE Select | NP_005553.2:p.Gln36Arg | |
NM_018891.3:c.107A>G | NP_061486.2:p.Gln36Arg |