Canonical Allele Identifier: CA2020991432
Gene: SLCO1B1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21178587G= , CM000674.2:g.21178587G= GRCh38
NC_000012.11:g.21331521G= , CM000674.1:g.21331521G= GRCh37
NC_000012.10:g.21222788G= NCBI36
NG_011745.1:g.52394G= , LRG_1022:g.52394G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.493G= MANE Select ENSP00000256958.2:p.Glu165=
ENST00000256958.2:c.493G= ENSP00000256958.2:p.Glu165=
NM_006446.4:c.493G= , LRG_1022t1:c.493G= NP_006437.3:p.Glu165=
NM_006446.5:c.493G= MANE Select NP_006437.3:p.Glu165=
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