HGVS | Genome Assembly |
---|---|
NC_000008.11:g.38148694C>A , CM000670.2:g.38148694C>A | GRCh38 |
NC_000008.10:g.38006212C>A , CM000670.1:g.38006212C>A | GRCh37 |
NC_000008.9:g.38125369C>A | NCBI36 |
NG_011827.1:g.7389G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000276449.9:c.125G>T MANE Select | ENSP00000276449.3:p.Gly42Val | |
ENST00000276449.8:c.125G>T | ENSP00000276449.3:p.Gly42Val | |
ENST00000520114.1:n.299G>T | ||
ENST00000521236.1:c.-154G>T | ENSP00000430030.1:n.-154G>T | |
ENST00000522050.1:c.61G>T | ||
NM_000349.2:c.125G>T | NP_000340.2:p.Gly42Val | |
XM_006716392.1:c.125G>T | XP_006716455.1:p.Gly42Val | |
NM_000349.3:c.125G>T MANE Select | NP_000340.2:p.Gly42Val |