HGVS | Genome Assembly |
---|---|
NC_000001.11:g.171652471G= , CM000663.2:g.171652471G= | GRCh38 |
NC_000001.10:g.171621611G= , CM000663.1:g.171621611G= | GRCh37 |
NC_000001.9:g.169888234G= | NCBI36 |
NG_008859.1:g.5163C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000037502.11:c.141C= MANE Select | ENSP00000037502.5:p.Cys47= | |
ENST00000638471.1:c.130+11C= | ENSP00000491206.1:n.130+11C= | |
ENST00000037502.10:c.141C= | ENSP00000037502.5:p.Cys47= | |
ENST00000614688.1:c.141C= | ENSP00000478680.1:p.Cys47= | |
NM_000261.1:c.141C= | NP_000252.1:p.Cys47= | |
NM_000261.2:c.141C= MANE Select | NP_000252.1:p.Cys47= |