Canonical Allele Identifier: CA233559921
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs952815153
gnomAD v3: 12-21174863-C-A
gnomAD v4: 12-21174863-C-A
MyVariant Identifiers: chr12:g.21174863C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21174863C>A , CM000674.2:g.21174863C>A GRCh38
NC_000012.11:g.21327797C>A , CM000674.1:g.21327797C>A GRCh37
NC_000012.10:g.21219064C>A NCBI36
NG_011745.1:g.48670C>A , LRG_1022:g.48670C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.359+154C>A MANE Select ENSP00000256958.2:n.359+154C>A
ENST00000256958.2:c.359+154C>A ENSP00000256958.2:n.359+154C>A
ENST00000543498.5:c.426-1913C>A
NM_006446.4:c.359+154C>A , LRG_1022t1:c.359+154C>A NP_006437.3:n.359+154C>A
NM_006446.5:c.359+154C>A MANE Select NP_006437.3:n.359+154C>A
Search 100 bp 5'
Search 100 bp 3'