HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94781861G>C , CM000672.2:g.94781861G>C | GRCh38 |
NC_000010.10:g.96541618G>C , CM000672.1:g.96541618G>C | GRCh37 |
NC_000010.9:g.96531608G>C | NCBI36 |
NG_008384.2:g.24156G>C | |
NG_008384.3:g.24181G>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000371321.9:c.683G>C MANE Select | ENSP00000360372.3:p.Gly228Ala | |
ENST00000645461.1:n.1736G>C | ||
ENST00000371321.7:c.683G>C | ENSP00000360372.3:p.Gly228Ala | |
ENST00000464755.1:c.1446G>C | ENSP00000483243.1:n.1446G>C | |
NM_000769.2:c.683G>C | NP_000760.1:p.Gly228Ala | |
NM_000769.4:c.683G>C MANE Select | NP_000760.1:p.Gly228Ala |