Canonical Allele Identifier: CA384106054
Gene: SLCO1B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.21349930C>G (hg19) chr12:g.21196996C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21196996C>G , CM000674.2:g.21196996C>G GRCh38
NC_000012.11:g.21349930C>G , CM000674.1:g.21349930C>G GRCh37
NC_000012.10:g.21241197C>G NCBI36
NG_011745.1:g.70803C>G , LRG_1022:g.70803C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.778C>G MANE Select ENSP00000256958.2:p.Leu260Val
ENST00000256958.2:c.778C>G ENSP00000256958.2:p.Leu260Val
NM_006446.4:c.778C>G , LRG_1022t1:c.778C>G NP_006437.3:p.Leu260Val
NM_006446.5:c.778C>G MANE Select NP_006437.3:p.Leu260Val
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