HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94029571G>T , CM000663.2:g.94029571G>T | GRCh38 |
NC_000001.10:g.94495127G>T , CM000663.1:g.94495127G>T | GRCh37 |
NC_000001.9:g.94267715G>T | NCBI36 |
NG_009073.1:g.96579C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370225.4:c.4413C>A MANE Select | ENSP00000359245.3:p.Thr1471= | |
ENST00000370225.3:c.4413C>A | ENSP00000359245.3:p.Thr1471= | |
ENST00000536513.5:c.789C>A | ENSP00000439707.2:p.Thr263= | |
NM_000350.2:c.4413C>A | NP_000341.2:p.Thr1471= | |
NM_000350.3:c.4413C>A MANE Select | NP_000341.2:p.Thr1471= |