Canonical Allele Identifier: CA2020991340
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1940847443
gnomAD v4: 12-21178434-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21178434A>T , CM000674.2:g.21178434A>T GRCh38
NC_000012.11:g.21331368A>T , CM000674.1:g.21331368A>T GRCh37
NC_000012.10:g.21222635A>T NCBI36
NG_011745.1:g.52241A>T , LRG_1022:g.52241A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.482-142A>T MANE Select ENSP00000256958.2:n.482-142A>T
ENST00000256958.2:c.482-142A>T ENSP00000256958.2:n.482-142A>T
NM_006446.4:c.482-142A>T , LRG_1022t1:c.482-142A>T NP_006437.3:n.482-142A>T
NM_006446.5:c.482-142A>T MANE Select NP_006437.3:n.482-142A>T
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