Canonical Allele Identifier: CA2020989626
Gene: SLCO1B1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21174629A= , CM000674.2:g.21174629A= GRCh38
NC_000012.11:g.21327563A= , CM000674.1:g.21327563A= GRCh37
NC_000012.10:g.21218830A= NCBI36
NG_011745.1:g.48436A= , LRG_1022:g.48436A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.279A= MANE Select ENSP00000256958.2:p.Arg93=
ENST00000256958.2:c.279A= ENSP00000256958.2:p.Arg93=
ENST00000543498.5:c.426-2147A=
NM_006446.4:c.279A= , LRG_1022t1:c.279A= NP_006437.3:p.Arg93=
NM_006446.5:c.279A= MANE Select NP_006437.3:p.Arg93=
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