Canonical Allele Identifier: CA2021001569
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1941149371
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21200886C>T , CM000674.2:g.21200886C>T GRCh38
NC_000012.11:g.21353820C>T , CM000674.1:g.21353820C>T GRCh37
NC_000012.10:g.21245087C>T NCBI36
NG_011745.1:g.74693C>T , LRG_1022:g.74693C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.1135+214C>T MANE Select ENSP00000256958.2:n.1135+214C>T
ENST00000256958.2:c.1135+214C>T ENSP00000256958.2:n.1135+214C>T
NM_006446.4:c.1135+214C>T , LRG_1022t1:c.1135+214C>T NP_006437.3:n.1135+214C>T
NM_006446.5:c.1135+214C>T MANE Select NP_006437.3:n.1135+214C>T
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Search 100 bp 3'