Canonical Allele Identifier: CA384106802
Gene: SLCO1B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.21353590G>C (hg19) chr12:g.21200656G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21200656G>C , CM000674.2:g.21200656G>C GRCh38
NC_000012.11:g.21353590G>C , CM000674.1:g.21353590G>C GRCh37
NC_000012.10:g.21244857G>C NCBI36
NG_011745.1:g.74463G>C , LRG_1022:g.74463G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.1119G>C MANE Select ENSP00000256958.2:p.Lys373Asn
ENST00000256958.2:c.1119G>C ENSP00000256958.2:p.Lys373Asn
NM_006446.4:c.1119G>C , LRG_1022t1:c.1119G>C NP_006437.3:p.Lys373Asn
NM_006446.5:c.1119G>C MANE Select NP_006437.3:p.Lys373Asn
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