Canonical Allele Identifier: CA2020999849
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1941098721
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21196932A>T , CM000674.2:g.21196932A>T GRCh38
NC_000012.11:g.21349866A>T , CM000674.1:g.21349866A>T GRCh37
NC_000012.10:g.21241133A>T NCBI36
NG_011745.1:g.70739A>T , LRG_1022:g.70739A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.728-14A>T MANE Select ENSP00000256958.2:n.728-14A>T
ENST00000256958.2:c.728-14A>T ENSP00000256958.2:n.728-14A>T
NM_006446.4:c.728-14A>T , LRG_1022t1:c.728-14A>T NP_006437.3:n.728-14A>T
NM_006446.5:c.728-14A>T MANE Select NP_006437.3:n.728-14A>T
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