Canonical Allele Identifier: CA478864267
Gene: SLCO1B1 HGNC NCBI

Linked Data

gnomAD v4: 12-21200515-C-T
COSMIC: COSM2004937
MyVariant Identifiers: chr12:g.21353449C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21200515C>T , CM000674.2:g.21200515C>T GRCh38
NC_000012.11:g.21353449C>T , CM000674.1:g.21353449C>T GRCh37
NC_000012.10:g.21244716C>T NCBI36
NG_011745.1:g.74322C>T , LRG_1022:g.74322C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.978C>T MANE Select ENSP00000256958.2:p.Phe326=
ENST00000256958.2:c.978C>T ENSP00000256958.2:p.Phe326=
NM_006446.4:c.978C>T , LRG_1022t1:c.978C>T NP_006437.3:p.Phe326=
NM_006446.5:c.978C>T MANE Select NP_006437.3:p.Phe326=
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