Canonical Allele Identifier: CA384105545
Gene: SLCO1B1 HGNC NCBI

Linked Data

gnomAD v4: 12-21178635-C-A
MyVariant Identifiers: chr12:g.21331569C>A (hg19) chr12:g.21178635C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21178635C>A , CM000674.2:g.21178635C>A GRCh38
NC_000012.11:g.21331569C>A , CM000674.1:g.21331569C>A GRCh37
NC_000012.10:g.21222836C>A NCBI36
NG_011745.1:g.52442C>A , LRG_1022:g.52442C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.541C>A MANE Select ENSP00000256958.2:p.Arg181Ser
ENST00000256958.2:c.541C>A ENSP00000256958.2:p.Arg181Ser
NM_006446.4:c.541C>A , LRG_1022t1:c.541C>A NP_006437.3:p.Arg181Ser
NM_006446.5:c.541C>A MANE Select NP_006437.3:p.Arg181Ser
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Search 100 bp 3'