Canonical Allele Identifier: CA384106755

Gene: SLCO1B1

Linked Data

• gnomAD v4: 12-21200634-A-G
• MyVariant Identifiers: chr12:g.21353568A>G (hg19) ; chr12:g.21200634A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21200634A>G , CM000674.2:g.21200634A>G	GRCh38
NC_000012.11:g.21353568A>G , CM000674.1:g.21353568A>G	GRCh37
NC_000012.10:g.21244835A>G	NCBI36
NG_011745.1:g.74441A>G , LRG_1022:g.74441A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256958.3:c.1097A>G MANE Select	ENSP00000256958.2:p.Gln366Arg
ENST00000256958.2:c.1097A>G	ENSP00000256958.2:p.Gln366Arg
NM_006446.4:c.1097A>G , LRG_1022t1:c.1097A>G	NP_006437.3:p.Gln366Arg
NM_006446.5:c.1097A>G MANE Select	NP_006437.3:p.Gln366Arg