Canonical Allele Identifier: CA233565425
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs146215585
gnomAD v2: 12-21368543-A-G
gnomAD v3: 12-21215609-A-G
gnomAD v4: 12-21215609-A-G
MyVariant Identifiers: chr12:g.21368543A>G (hg19) chr12:g.21215609A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21215609A>G , CM000674.2:g.21215609A>G GRCh38
NC_000012.11:g.21368543A>G , CM000674.1:g.21368543A>G GRCh37
NC_000012.10:g.21259810A>G NCBI36
NG_011745.1:g.89416A>G , LRG_1022:g.89416A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.1498-1510A>G MANE Select ENSP00000256958.2:n.1498-1510A>G
ENST00000256958.2:c.1498-1510A>G ENSP00000256958.2:n.1498-1510A>G
NM_006446.4:c.1498-1510A>G , LRG_1022t1:c.1498-1510A>G NP_006437.3:n.1498-1510A>G
NM_006446.5:c.1498-1510A>G MANE Select NP_006437.3:n.1498-1510A>G
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