Canonical Allele Identifier: CA2020999883
Gene: SLCO1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21196988C= , CM000674.2:g.21196988C= GRCh38
NC_000012.11:g.21349922C= , CM000674.1:g.21349922C= GRCh37
NC_000012.10:g.21241189C= NCBI36
NG_011745.1:g.70795C= , LRG_1022:g.70795C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.770C= MANE Select ENSP00000256958.2:p.Ala257=
ENST00000256958.2:c.770C= ENSP00000256958.2:p.Ala257=
NM_006446.4:c.770C= , LRG_1022t1:c.770C= NP_006437.3:p.Ala257=
NM_006446.5:c.770C= MANE Select NP_006437.3:p.Ala257=