HGVS | Genome Assembly |
---|---|
NC_000009.12:g.101686830C>G , CM000671.2:g.101686830C>G | GRCh38 |
NC_000009.11:g.104449112C>G , CM000671.1:g.104449112C>G | GRCh37 |
NC_000009.10:g.103488933C>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361820.6:c.1070G>C MANE Select | ENSP00000355155.3:p.Gly357Ala | |
ENST00000361820.3:c.1070G>C | ENSP00000355155.3:p.Gly357Ala | |
NM_133445.2:c.1070G>C | NP_597702.2:p.Gly357Ala | |
XM_011518211.1:c.1070G>C | XP_011516513.1:p.Gly357Ala | |
XM_011518212.1:c.1070G>C | XP_011516514.1:p.Gly357Ala | |
XR_929711.1:n.1157G>C | ||
XM_011518211.2:c.1070G>C | XP_011516513.1:p.Gly357Ala | |
NM_133445.3:c.1070G>C MANE Select | NP_597702.2:p.Gly357Ala |