Canonical Allele Identifier: CA686353431

Gene: SLCO1B1

Linked Data

• dbSNP Id: rs1295205302
• MyVariant Identifiers: chr12:g.21327959C>T (hg19) ; chr12:g.21175025C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21175025C>T , CM000674.2:g.21175025C>T	GRCh38
NC_000012.11:g.21327959C>T , CM000674.1:g.21327959C>T	GRCh37
NC_000012.10:g.21219226C>T	NCBI36
NG_011745.1:g.48832C>T , LRG_1022:g.48832C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256958.3:c.359+316C>T MANE Select	ENSP00000256958.2:n.359+316C>T
ENST00000256958.2:c.359+316C>T	ENSP00000256958.2:n.359+316C>T
ENST00000543498.5:c.426-1751C>T
NM_006446.4:c.359+316C>T , LRG_1022t1:c.359+316C>T	NP_006437.3:n.359+316C>T
NM_006446.5:c.359+316C>T MANE Select	NP_006437.3:n.359+316C>T