Canonical Allele Identifier: CA603657679

Gene: SLCO1B1

Linked Data

• dbSNP Id: rs886049144
• gnomAD v2: 12-21329695-G-C
• gnomAD v4: 12-21176761-G-C
• MyVariant Identifiers: chr12:g.21329695G>C (hg19) ; chr12:g.21176761G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21176761G>C , CM000674.2:g.21176761G>C	GRCh38
NC_000012.11:g.21329695G>C , CM000674.1:g.21329695G>C	GRCh37
NC_000012.10:g.21220962G>C	NCBI36
NG_011745.1:g.50568G>C , LRG_1022:g.50568G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256958.3:c.360-15G>C MANE Select	ENSP00000256958.2:n.360-15G>C
ENST00000256958.2:c.360-15G>C	ENSP00000256958.2:n.360-15G>C
ENST00000543498.5:c.426-15G>C
NM_006446.4:c.360-15G>C , LRG_1022t1:c.360-15G>C	NP_006437.3:n.360-15G>C
NM_006446.5:c.360-15G>C MANE Select	NP_006437.3:n.360-15G>C