HGVS | Genome Assembly |
---|---|
NC_000013.11:g.110169708C>G , CM000675.2:g.110169708C>G | GRCh38 |
NC_000013.10:g.110822055C>G , CM000675.1:g.110822055C>G | GRCh37 |
NC_000013.9:g.109620056C>G | NCBI36 |
NG_011544.2:g.142442G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375820.10:c.3797G>C MANE Select | ENSP00000364979.4:p.Gly1266Ala | |
ENST00000375820.8:c.3797G>C | ENSP00000364979.4:p.Gly1266Ala | |
NM_001845.5:c.3797G>C | NP_001836.3:p.Gly1266Ala | |
XM_011521048.1:c.3605G>C | XP_011519350.1:p.Gly1202Ala | |
XM_011521048.2:c.3605G>C | XP_011519350.1:p.Gly1202Ala | |
NM_001845.6:c.3797G>C MANE Select | NP_001836.3:p.Gly1266Ala |