Canonical Allele Identifier: CA2020990571
Gene: SLCO1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21176697A= , CM000674.2:g.21176697A= GRCh38
NC_000012.11:g.21329631A= , CM000674.1:g.21329631A= GRCh37
NC_000012.10:g.21220898A= NCBI36
NG_011745.1:g.50504A= , LRG_1022:g.50504A=

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.360-79A= MANE Select ENSP00000256958.2:n.360-79A=
ENST00000256958.2:c.360-79A= ENSP00000256958.2:n.360-79A=
ENST00000543498.5:c.426-79A=
NM_006446.4:c.360-79A= , LRG_1022t1:c.360-79A= NP_006437.3:n.360-79A=
NM_006446.5:c.360-79A= MANE Select NP_006437.3:n.360-79A=