Canonical Allele Identifier: CA384105507
Gene: SLCO1B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21178618T>C , CM000674.2:g.21178618T>C GRCh38
NC_000012.11:g.21331552T>C , CM000674.1:g.21331552T>C GRCh37
NC_000012.10:g.21222819T>C NCBI36
NG_011745.1:g.52425T>C , LRG_1022:g.52425T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.524T>C MANE Select ENSP00000256958.2:p.Phe175Ser
ENST00000256958.2:c.524T>C ENSP00000256958.2:p.Phe175Ser
NM_006446.4:c.524T>C , LRG_1022t1:c.524T>C NP_006437.3:p.Phe175Ser
NM_006446.5:c.524T>C MANE Select NP_006437.3:p.Phe175Ser