Canonical Allele Identifier: CA686380553
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1302116616
MyVariant Identifiers: chr12:g.21369036C>A (hg19) chr12:g.21216102C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21216102C>A , CM000674.2:g.21216102C>A GRCh38
NC_000012.11:g.21369036C>A , CM000674.1:g.21369036C>A GRCh37
NC_000012.10:g.21260303C>A NCBI36
NG_011745.1:g.89909C>A , LRG_1022:g.89909C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.1498-1017C>A MANE Select ENSP00000256958.2:n.1498-1017C>A
ENST00000256958.2:c.1498-1017C>A ENSP00000256958.2:n.1498-1017C>A
NM_006446.4:c.1498-1017C>A , LRG_1022t1:c.1498-1017C>A NP_006437.3:n.1498-1017C>A
NM_006446.5:c.1498-1017C>A MANE Select NP_006437.3:n.1498-1017C>A
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