Canonical Allele Identifier: CA2021009625
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1941351826
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21215866dup , CM000674.2:g.21215866dup GRCh38
NC_000012.11:g.21368800dup , CM000674.1:g.21368800dup GRCh37
NC_000012.10:g.21260067dup NCBI36
NG_011745.1:g.89673dup , LRG_1022:g.89673dup

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.1498-1253dup MANE Select ENSP00000256958.2:n.1498-1253dup
ENST00000256958.2:c.1498-1253dup ENSP00000256958.2:n.1498-1253dup
NM_006446.4:c.1498-1253dup , LRG_1022t1:c.1498-1253dup NP_006437.3:n.1498-1253dup
NM_006446.5:c.1498-1253dup MANE Select NP_006437.3:n.1498-1253dup
Search 100 bp 5'
Search 100 bp 3'