Canonical Allele Identifier: CA603658500
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1565437239
gnomAD v2: 12-21353607-G-GT
gnomAD v4: 12-21200673-G-GT
MyVariant Identifiers: chr12:g.21353607_21353608insT (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21200674dup , CM000674.2:g.21200674dup GRCh38
NC_000012.11:g.21353608dup , CM000674.1:g.21353608dup GRCh37
NC_000012.10:g.21244875dup NCBI36
NG_011745.1:g.74481dup , LRG_1022:g.74481dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.1135+2dup MANE Select ENSP00000256958.2:n.1135+2dup
ENST00000256958.2:c.1135+2dup ENSP00000256958.2:n.1135+2dup
NM_006446.4:c.1135+2dup , LRG_1022t1:c.1135+2dup NP_006437.3:n.1135+2dup
NM_006446.5:c.1135+2dup MANE Select NP_006437.3:n.1135+2dup
Search 100 bp 5'
Search 100 bp 3'