Canonical Allele Identifier: CA686352883
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1310954750
MyVariant Identifiers: chr12:g.21327348del (hg19) chr12:g.21174414del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21174415del , CM000674.2:g.21174415del GRCh38
NC_000012.11:g.21327349del , CM000674.1:g.21327349del GRCh37
NC_000012.10:g.21218616del NCBI36
NG_011745.1:g.48222del , LRG_1022:g.48222del

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.227-162del MANE Select ENSP00000256958.2:n.227-162del
ENST00000256958.2:c.227-162del ENSP00000256958.2:n.227-162del
ENST00000543498.5:c.426-2361del
NM_006446.4:c.227-162del , LRG_1022t1:c.227-162del NP_006437.3:n.227-162del
NM_006446.5:c.227-162del MANE Select NP_006437.3:n.227-162del
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