Canonical Allele Identifier: CA2020999779
Gene: SLCO1B1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21196786G= , CM000674.2:g.21196786G= GRCh38
NC_000012.11:g.21349720G= , CM000674.1:g.21349720G= GRCh37
NC_000012.10:g.21240987G= NCBI36
NG_011745.1:g.70593G= , LRG_1022:g.70593G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.728-160G= MANE Select ENSP00000256958.2:n.728-160G=
ENST00000256958.2:c.728-160G= ENSP00000256958.2:n.728-160G=
NM_006446.4:c.728-160G= , LRG_1022t1:c.728-160G= NP_006437.3:n.728-160G=
NM_006446.5:c.728-160G= MANE Select NP_006437.3:n.728-160G=
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