HGVS | Genome Assembly |
---|---|
NC_000016.10:g.173578T>A , CM000678.2:g.173578T>A | GRCh38 |
NC_000016.9:g.223577T>A , CM000678.1:g.223577T>A | GRCh37 |
NC_000016.8:g.163577T>A | NCBI36 |
NG_000006.1:g.34441T>A | |
NG_059186.1:g.1928T>A | |
NG_059271.1:g.5732T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000251595.11:c.407T>A MANE Select | ENSP00000251595.6:p.Val136Glu | |
ENST00000251595.10:c.407T>A | ENSP00000251595.6:p.Val136Glu | |
ENST00000397806.1:c.311T>A | ENSP00000380908.1:p.Val104Glu | |
ENST00000482565.1:n.543T>A | ||
NM_000517.4:c.407T>A | NP_000508.1:p.Val136Glu | |
NM_000517.6:c.407T>A MANE Select | NP_000508.1:p.Val136Glu |