Canonical Allele Identifier: CA233559973
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs71581980
gnomAD v2: 12-21327840-AC-A
gnomAD v3: 12-21174906-AC-A
gnomAD v4: 12-21174906-AC-A
MyVariant Identifiers: chr12:g.21327841del (hg19) chr12:g.21174907del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21174907del , CM000674.2:g.21174907del GRCh38
NC_000012.11:g.21327841del , CM000674.1:g.21327841del GRCh37
NC_000012.10:g.21219108del NCBI36
NG_011745.1:g.48714del , LRG_1022:g.48714del

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.359+198del MANE Select ENSP00000256958.2:n.359+198del
ENST00000256958.2:c.359+198del ENSP00000256958.2:n.359+198del
ENST00000543498.5:c.426-1869del
NM_006446.4:c.359+198del , LRG_1022t1:c.359+198del NP_006437.3:n.359+198del
NM_006446.5:c.359+198del MANE Select NP_006437.3:n.359+198del
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