Canonical Allele Identifier: CA2020989713
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1940799855
gnomAD v4: 12-21174825-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21174825T>C , CM000674.2:g.21174825T>C GRCh38
NC_000012.11:g.21327759T>C , CM000674.1:g.21327759T>C GRCh37
NC_000012.10:g.21219026T>C NCBI36
NG_011745.1:g.48632T>C , LRG_1022:g.48632T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.359+116T>C MANE Select ENSP00000256958.2:n.359+116T>C
ENST00000256958.2:c.359+116T>C ENSP00000256958.2:n.359+116T>C
ENST00000543498.5:c.426-1951T>C
NM_006446.4:c.359+116T>C , LRG_1022t1:c.359+116T>C NP_006437.3:n.359+116T>C
NM_006446.5:c.359+116T>C MANE Select NP_006437.3:n.359+116T>C
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