HGVS | Genome Assembly |
---|---|
NC_000001.11:g.171652346T>A , CM000663.2:g.171652346T>A | GRCh38 |
NC_000001.10:g.171621486T>A , CM000663.1:g.171621486T>A | GRCh37 |
NC_000001.9:g.169888109T>A | NCBI36 |
NG_008859.1:g.5288A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000037502.11:c.266A>T MANE Select | ENSP00000037502.5:p.Lys89Ile | |
ENST00000638471.1:c.130+136A>T | ENSP00000491206.1:n.130+136A>T | |
ENST00000037502.10:c.266A>T | ENSP00000037502.5:p.Lys89Ile | |
ENST00000614688.1:c.266A>T | ENSP00000478680.1:p.Lys89Ile | |
NM_000261.1:c.266A>T | NP_000252.1:p.Lys89Ile | |
NM_000261.2:c.266A>T MANE Select | NP_000252.1:p.Lys89Ile |