HGVS | Genome Assembly |
---|---|
NC_000017.11:g.42536379T>C , CM000679.2:g.42536379T>C | GRCh38 |
NC_000017.10:g.40688397T>C , CM000679.1:g.40688397T>C | GRCh37 |
NC_000017.9:g.37941923T>C | NCBI36 |
NG_011552.1:g.5447T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000225927.7:c.107T>C MANE Select | ENSP00000225927.1:p.Val36Ala | |
ENST00000225927.6:c.107T>C | ENSP00000225927.1:p.Val36Ala | |
NM_000263.3:c.107T>C | NP_000254.2:p.Val36Ala | |
XM_024450771.1:c.107T>C | XP_024306539.1:p.Val36Ala | |
NM_000263.4:c.107T>C MANE Select | NP_000254.2:p.Val36Ala |