HGVS | Genome Assembly |
---|---|
NC_000016.10:g.173285G>C , CM000678.2:g.173285G>C | GRCh38 |
NC_000016.9:g.223284G>C , CM000678.1:g.223284G>C | GRCh37 |
NC_000016.8:g.163284G>C | NCBI36 |
NG_000006.1:g.34148G>C | |
NG_059186.1:g.1635G>C | |
NG_059271.1:g.5439G>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000251595.11:c.256G>C MANE Select | ENSP00000251595.6:p.Asp86His | |
ENST00000251595.10:c.256G>C | ENSP00000251595.6:p.Asp86His | |
ENST00000397806.1:c.160G>C | ENSP00000380908.1:p.Asp54His | |
ENST00000482565.1:n.392G>C | ||
ENST00000484216.1:n.225G>C | ||
NM_000517.4:c.256G>C | NP_000508.1:p.Asp86His | |
NM_000517.6:c.256G>C MANE Select | NP_000508.1:p.Asp86His |