HGVS | Genome Assembly |
---|---|
NC_000013.11:g.27924378G>C , CM000675.2:g.27924378G>C | GRCh38 |
NC_000013.10:g.28498515G>C , CM000675.1:g.28498515G>C | GRCh37 |
NC_000013.9:g.27396515G>C | NCBI36 |
NG_008183.1:g.9348G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000381033.5:c.529G>C MANE Select | ENSP00000370421.4:p.Val177Leu | |
ENST00000381033.4:c.529G>C | ENSP00000370421.4:p.Val177Leu | |
NM_000209.3:c.529G>C | NP_000200.1:p.Val177Leu | |
NM_000209.4:c.529G>C MANE Select | NP_000200.1:p.Val177Leu |