Canonical Allele Identifier: CA945496348
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1940800530

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21174886_21174905dup , CM000674.2:g.21174886_21174905dup GRCh38
NC_000012.11:g.21327820_21327839dup , CM000674.1:g.21327820_21327839dup GRCh37
NC_000012.10:g.21219087_21219106dup NCBI36
NG_011745.1:g.48693_48712dup , LRG_1022:g.48693_48712dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.359+177_359+196dup MANE Select ENSP00000256958.2:n.359+177_359+196dup
ENST00000256958.2:c.359+177_359+196dup ENSP00000256958.2:n.359+177_359+196dup
ENST00000543498.5:c.426-1890_426-1871dup
NM_006446.4:c.359+177_359+196dup , LRG_1022t1:c.359+177_359+196dup NP_006437.3:n.359+177_359+196dup
NM_006446.5:c.359+177_359+196dup MANE Select NP_006437.3:n.359+177_359+196dup