Canonical Allele Identifier: CA384104352
Gene: SLCO1B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.21327628A>G (hg19) chr12:g.21174694A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21174694A>G , CM000674.2:g.21174694A>G GRCh38
NC_000012.11:g.21327628A>G , CM000674.1:g.21327628A>G GRCh37
NC_000012.10:g.21218895A>G NCBI36
NG_011745.1:g.48501A>G , LRG_1022:g.48501A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.344A>G MANE Select ENSP00000256958.2:p.His115Arg
ENST00000256958.2:c.344A>G ENSP00000256958.2:p.His115Arg
ENST00000543498.5:c.426-2082A>G
NM_006446.4:c.344A>G , LRG_1022t1:c.344A>G NP_006437.3:p.His115Arg
NM_006446.5:c.344A>G MANE Select NP_006437.3:p.His115Arg
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