Canonical Allele Identifier: CA384105138
Gene: SLCO1B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21178596T>C , CM000674.2:g.21178596T>C GRCh38
NC_000012.11:g.21331530T>C , CM000674.1:g.21331530T>C GRCh37
NC_000012.10:g.21222797T>C NCBI36
NG_011745.1:g.52403T>C , LRG_1022:g.52403T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.502T>C MANE Select ENSP00000256958.2:p.Ser168Pro
ENST00000256958.2:c.502T>C ENSP00000256958.2:p.Ser168Pro
NM_006446.4:c.502T>C , LRG_1022t1:c.502T>C NP_006437.3:p.Ser168Pro
NM_006446.5:c.502T>C MANE Select NP_006437.3:p.Ser168Pro