Canonical Allele Identifier: CA233565622
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1002542569

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21215728dup , CM000674.2:g.21215728dup GRCh38
NC_000012.11:g.21368662dup , CM000674.1:g.21368662dup GRCh37
NC_000012.10:g.21259929dup NCBI36
NG_011745.1:g.89535dup , LRG_1022:g.89535dup

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.1498-1391dup MANE Select ENSP00000256958.2:n.1498-1391dup
ENST00000256958.2:c.1498-1391dup ENSP00000256958.2:n.1498-1391dup
NM_006446.4:c.1498-1391dup , LRG_1022t1:c.1498-1391dup NP_006437.3:n.1498-1391dup
NM_006446.5:c.1498-1391dup MANE Select NP_006437.3:n.1498-1391dup