Canonical Allele Identifier: CA686355174

Gene: SLCO1B1

Linked Data

• dbSNP Id: rs1347059928
• gnomAD v3: 12-21178396-T-C
• gnomAD v4: 12-21178396-T-C
• MyVariant Identifiers: chr12:g.21331330T>C (hg19) ; chr12:g.21178396T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21178396T>C , CM000674.2:g.21178396T>C	GRCh38
NC_000012.11:g.21331330T>C , CM000674.1:g.21331330T>C	GRCh37
NC_000012.10:g.21222597T>C	NCBI36
NG_011745.1:g.52203T>C , LRG_1022:g.52203T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256958.3:c.482-180T>C MANE Select	ENSP00000256958.2:n.482-180T>C
ENST00000256958.2:c.482-180T>C	ENSP00000256958.2:n.482-180T>C
NM_006446.4:c.482-180T>C , LRG_1022t1:c.482-180T>C	NP_006437.3:n.482-180T>C
NM_006446.5:c.482-180T>C MANE Select	NP_006437.3:n.482-180T>C