Canonical Allele Identifier: CA478866612

Gene: SLCO1B1

Linked Data

• MyVariant Identifiers: chr12:g.21327614G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21174680G>A , CM000674.2:g.21174680G>A	GRCh38
NC_000012.11:g.21327614G>A , CM000674.1:g.21327614G>A	GRCh37
NC_000012.10:g.21218881G>A	NCBI36
NG_011745.1:g.48487G>A , LRG_1022:g.48487G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256958.3:c.330G>A MANE Select	ENSP00000256958.2:p.Leu110=
ENST00000256958.2:c.330G>A	ENSP00000256958.2:p.Leu110=
ENST00000543498.5:c.426-2096G>A
NM_006446.4:c.330G>A , LRG_1022t1:c.330G>A	NP_006437.3:p.Leu110=
NM_006446.5:c.330G>A MANE Select	NP_006437.3:p.Leu110=