Canonical Allele Identifier: CA686380346

Gene: SLCO1B1

Linked Data

• dbSNP Id: rs1319398375
• gnomAD v3: 12-21215765-G-C
• gnomAD v4: 12-21215765-G-C
• MyVariant Identifiers: chr12:g.21368699G>C (hg19) ; chr12:g.21215765G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21215765G>C , CM000674.2:g.21215765G>C	GRCh38
NC_000012.11:g.21368699G>C , CM000674.1:g.21368699G>C	GRCh37
NC_000012.10:g.21259966G>C	NCBI36
NG_011745.1:g.89572G>C , LRG_1022:g.89572G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000256958.3:c.1498-1354G>C MANE Select	ENSP00000256958.2:n.1498-1354G>C
ENST00000256958.2:c.1498-1354G>C	ENSP00000256958.2:n.1498-1354G>C
NM_006446.4:c.1498-1354G>C , LRG_1022t1:c.1498-1354G>C	NP_006437.3:n.1498-1354G>C
NM_006446.5:c.1498-1354G>C MANE Select	NP_006437.3:n.1498-1354G>C