Canonical Allele Identifier: CA2020975206
Gene: SLCO1B1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21138577T= , CM000674.2:g.21138577T= GRCh38
NC_000012.11:g.21291511T= , CM000674.1:g.21291511T= GRCh37
NC_000012.10:g.21182778T= NCBI36
NG_011745.1:g.12384T= , LRG_1022:g.12384T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.-61-2937T= MANE Select ENSP00000256958.2:n.-61-2937T=
ENST00000256958.2:c.-61-2937T= ENSP00000256958.2:n.-61-2937T=
ENST00000543498.5:c.281-2937T=
ENST00000585342.5:c.485-2937T= ENSP00000467594.1:n.485-2937T=
ENST00000590779.5:c.491-2937T=
ENST00000592513.1:c.472-2937T=
NM_006446.4:c.-61-2937T= , LRG_1022t1:c.-61-2937T= NP_006437.3:n.-61-2937T=
NM_006446.5:c.-61-2937T= MANE Select NP_006437.3:n.-61-2937T=
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