Canonical Allele Identifier: CA384106485
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1191553413
gnomAD v2: 12-21353444-T-C
gnomAD v4: 12-21200510-T-C
MyVariant Identifiers: chr12:g.21353444T>C (hg19) chr12:g.21200510T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21200510T>C , CM000674.2:g.21200510T>C GRCh38
NC_000012.11:g.21353444T>C , CM000674.1:g.21353444T>C GRCh37
NC_000012.10:g.21244711T>C NCBI36
NG_011745.1:g.74317T>C , LRG_1022:g.74317T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.973T>C MANE Select ENSP00000256958.2:p.Phe325Leu
ENST00000256958.2:c.973T>C ENSP00000256958.2:p.Phe325Leu
NM_006446.4:c.973T>C , LRG_1022t1:c.973T>C NP_006437.3:p.Phe325Leu
NM_006446.5:c.973T>C MANE Select NP_006437.3:p.Phe325Leu
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