Canonical Allele Identifier: CA1983218010
Gene: SLCO2B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.75196561C= , CM000673.2:g.75196561C= GRCh38
NC_000011.9:g.74907606C= , CM000673.1:g.74907606C= GRCh37
NC_000011.8:g.74585254C= NCBI36
NG_027921.1:g.50575C=

Transcript Alleles

HGVS Amino-acid change
ENST00000289575.10:c.1481C= MANE Select ENSP00000289575.5:p.Ser494=
ENST00000289575.9:c.1481C= ENSP00000289575.5:p.Ser494=
ENST00000428359.6:c.1415C= ENSP00000388912.2:p.Ser472=
ENST00000454962.6:c.800C= ENSP00000389653.2:p.Ser267=
ENST00000525650.5:c.1049C= ENSP00000436324.1:p.Ser350=
ENST00000528108.1:n.287C=
ENST00000530012.1:n.308C=
ENST00000531756.5:n.1028C=
ENST00000532236.5:c.1133C= ENSP00000434112.1:p.Ser378=
NM_001145211.2:c.1415C= NP_001138683.1:p.Ser472=
NM_001145212.2:c.1049C= NP_001138684.1:p.Ser350=
NM_007256.4:c.1481C= NP_009187.1:p.Ser494=
XM_017017157.1:c.1487C= XP_016872646.1:p.Ser496=
NM_001145211.3:c.1415C= NP_001138683.1:p.Ser472=
NM_001145212.3:c.1049C= NP_001138684.1:p.Ser350=
NM_007256.5:c.1481C= MANE Select NP_009187.1:p.Ser494=