Canonical Allele Identifier: CA384105145
Gene: SLCO1B1 HGNC NCBI

Linked Data

gnomAD v4: 12-21178597-C-T
MyVariant Identifiers: chr12:g.21331531C>T (hg19) chr12:g.21178597C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21178597C>T , CM000674.2:g.21178597C>T GRCh38
NC_000012.11:g.21331531C>T , CM000674.1:g.21331531C>T GRCh37
NC_000012.10:g.21222798C>T NCBI36
NG_011745.1:g.52404C>T , LRG_1022:g.52404C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.503C>T MANE Select ENSP00000256958.2:p.Ser168Leu
ENST00000256958.2:c.503C>T ENSP00000256958.2:p.Ser168Leu
NM_006446.4:c.503C>T , LRG_1022t1:c.503C>T NP_006437.3:p.Ser168Leu
NM_006446.5:c.503C>T MANE Select NP_006437.3:p.Ser168Leu
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