HGVS | Genome Assembly |
---|---|
NC_000004.12:g.99420779G>T , CM000666.2:g.99420779G>T | GRCh38 |
NC_000004.11:g.100341936G>T , CM000666.1:g.100341936G>T | GRCh37 |
NC_000004.10:g.100560959G>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000437033.7:c.579C>A MANE Select | ENSP00000414254.2:p.Ser193= | |
ENST00000209665.8:c.615C>A | ENSP00000209665.4:p.Ser205= | |
ENST00000437033.6:c.579C>A | ENSP00000414254.2:p.Ser193= | |
ENST00000476959.5:c.639C>A | ENSP00000420269.1:p.Ser213= | |
ENST00000482593.5:c.408C>A | ENSP00000420613.1:p.Ser136= | |
NM_000673.4:c.615C>A | NP_000664.2:p.Ser205= | |
NM_001166504.1:c.639C>A | NP_001159976.1:p.Ser213= | |
NM_000673.7:c.579C>A MANE Select | NP_000664.3:p.Ser193= | |
NM_001166504.2:c.639C>A | NP_001159976.1:p.Ser213= |