Canonical Allele Identifier: CA384106798
Gene: SLCO1B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.21353588A>T (hg19) chr12:g.21200654A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21200654A>T , CM000674.2:g.21200654A>T GRCh38
NC_000012.11:g.21353588A>T , CM000674.1:g.21353588A>T GRCh37
NC_000012.10:g.21244855A>T NCBI36
NG_011745.1:g.74461A>T , LRG_1022:g.74461A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.1117A>T MANE Select ENSP00000256958.2:p.Lys373Ter
ENST00000256958.2:c.1117A>T ENSP00000256958.2:p.Lys373Ter
NM_006446.4:c.1117A>T , LRG_1022t1:c.1117A>T NP_006437.3:p.Lys373Ter
NM_006446.5:c.1117A>T MANE Select NP_006437.3:p.Lys373Ter
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