Canonical Allele Identifier: CA603657600
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1200508714
gnomAD v2: 12-21327943-A-AT
gnomAD v3: 12-21175009-A-AT
gnomAD v4: 12-21175009-A-AT
MyVariant Identifiers: chr12:g.21327943_21327944insT (hg19) chr12:g.21175009_21175010insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21175015dup , CM000674.2:g.21175015dup GRCh38
NC_000012.11:g.21327949dup , CM000674.1:g.21327949dup GRCh37
NC_000012.10:g.21219216dup NCBI36
NG_011745.1:g.48822dup , LRG_1022:g.48822dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.359+306dup MANE Select ENSP00000256958.2:n.359+306dup
ENST00000256958.2:c.359+306dup ENSP00000256958.2:n.359+306dup
ENST00000543498.5:c.426-1761dup
NM_006446.4:c.359+306dup , LRG_1022t1:c.359+306dup NP_006437.3:n.359+306dup
NM_006446.5:c.359+306dup MANE Select NP_006437.3:n.359+306dup
Search 100 bp 5'
Search 100 bp 3'