Canonical Allele Identifier: CA6476661

Gene: SLCO1B1

Linked Data

• dbSNP Id: rs767074562
• ExAC: 12:21327663 A / AC
• gnomAD v2: 12-21327663-A-AC
• gnomAD v3: 12-21174729-A-AC
• gnomAD v4: 12-21174729-A-AC
• MyVariant Identifiers: chr12:g.21327663_21327664insC (hg19) ; chr12:g.21174729_21174730insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21174729_21174730insC , CM000674.2:g.21174729_21174730insC	GRCh38
NC_000012.11:g.21327663_21327664insC , CM000674.1:g.21327663_21327664insC	GRCh37
NC_000012.10:g.21218930_21218931insC	NCBI36
NG_011745.1:g.48536_48537insC , LRG_1022:g.48536_48537insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256958.3:c.359+20_359+21insC MANE Select	ENSP00000256958.2:n.359+20_359+21insC
ENST00000256958.2:c.359+20_359+21insC	ENSP00000256958.2:n.359+20_359+21insC
ENST00000543498.5:c.426-2047_426-2046insC
NM_006446.4:c.359+20_359+21insC , LRG_1022t1:c.359+20_359+21insC	NP_006437.3:n.359+20_359+21insC
NM_006446.5:c.359+20_359+21insC MANE Select	NP_006437.3:n.359+20_359+21insC