Canonical Allele Identifier: CA603657756
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1249194283

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21178553G>A , CM000674.2:g.21178553G>A GRCh38
NC_000012.11:g.21331487G>A , CM000674.1:g.21331487G>A GRCh37
NC_000012.10:g.21222754G>A NCBI36
NG_011745.1:g.52360G>A , LRG_1022:g.52360G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.482-23G>A MANE Select ENSP00000256958.2:n.482-23G>A
ENST00000256958.2:c.482-23G>A ENSP00000256958.2:n.482-23G>A
NM_006446.4:c.482-23G>A , LRG_1022t1:c.482-23G>A NP_006437.3:n.482-23G>A
NM_006446.5:c.482-23G>A MANE Select NP_006437.3:n.482-23G>A