Canonical Allele Identifier: CA2020989652
Gene: SLCO1B1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21174685C= , CM000674.2:g.21174685C= GRCh38
NC_000012.11:g.21327619C= , CM000674.1:g.21327619C= GRCh37
NC_000012.10:g.21218886C= NCBI36
NG_011745.1:g.48492C= , LRG_1022:g.48492C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.335C= MANE Select ENSP00000256958.2:p.Ala112=
ENST00000256958.2:c.335C= ENSP00000256958.2:p.Ala112=
ENST00000543498.5:c.426-2091C=
NM_006446.4:c.335C= , LRG_1022t1:c.335C= NP_006437.3:p.Ala112=
NM_006446.5:c.335C= MANE Select NP_006437.3:p.Ala112=
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