Canonical Allele Identifier: CA6476692

Gene: SLCO1B1

Linked Data

• dbSNP Id: rs140730264
• ExAC: 12:21329824 G / A
• gnomAD v2: 12-21329824-G-A
• gnomAD v3: 12-21176890-G-A
• gnomAD v4: 12-21176890-G-A
• MyVariant Identifiers: chr12:g.21329824G>A (hg19) ; chr12:g.21176890G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21176890G>A , CM000674.2:g.21176890G>A	GRCh38
NC_000012.11:g.21329824G>A , CM000674.1:g.21329824G>A	GRCh37
NC_000012.10:g.21221091G>A	NCBI36
NG_011745.1:g.50697G>A , LRG_1022:g.50697G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000256958.3:c.474G>A MANE Select	ENSP00000256958.2:p.Val158=
ENST00000256958.2:c.474G>A	ENSP00000256958.2:p.Val158=
ENST00000543498.5:c.540G>A
NM_006446.4:c.474G>A , LRG_1022t1:c.474G>A	NP_006437.3:p.Val158=
NM_006446.5:c.474G>A MANE Select	NP_006437.3:p.Val158=