Canonical Allele Identifier: CA384104817
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1370506945
gnomAD v2: 12-21329747-G-C
gnomAD v4: 12-21176813-G-C
MyVariant Identifiers: chr12:g.21329747G>C (hg19) chr12:g.21176813G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21176813G>C , CM000674.2:g.21176813G>C GRCh38
NC_000012.11:g.21329747G>C , CM000674.1:g.21329747G>C GRCh37
NC_000012.10:g.21221014G>C NCBI36
NG_011745.1:g.50620G>C , LRG_1022:g.50620G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.397G>C MANE Select ENSP00000256958.2:p.Glu133Gln
ENST00000256958.2:c.397G>C ENSP00000256958.2:p.Glu133Gln
ENST00000543498.5:c.463G>C
NM_006446.4:c.397G>C , LRG_1022t1:c.397G>C NP_006437.3:p.Glu133Gln
NM_006446.5:c.397G>C MANE Select NP_006437.3:p.Glu133Gln
Search 100 bp 5'
Search 100 bp 3'