Canonical Allele Identifier: CA2617895497
Gene: SLCO1B1 HGNC NCBI

Linked Data

gnomAD v4: 12-21200490-AT-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21200495del , CM000674.2:g.21200495del GRCh38
NC_000012.11:g.21353429del , CM000674.1:g.21353429del GRCh37
NC_000012.10:g.21244696del NCBI36
NG_011745.1:g.74302del , LRG_1022:g.74302del

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.971-13del MANE Select ENSP00000256958.2:n.971-13del
ENST00000256958.2:c.971-13del ENSP00000256958.2:n.971-13del
NM_006446.4:c.971-13del , LRG_1022t1:c.971-13del NP_006437.3:n.971-13del
NM_006446.5:c.971-13del MANE Select NP_006437.3:n.971-13del
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