Canonical Allele Identifier: CA686355266
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1472403104
gnomAD v4: 12-21178534-TA-T
MyVariant Identifiers: chr12:g.21331469del (hg19) chr12:g.21178535del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21178538del , CM000674.2:g.21178538del GRCh38
NC_000012.11:g.21331472del , CM000674.1:g.21331472del GRCh37
NC_000012.10:g.21222739del NCBI36
NG_011745.1:g.52345del , LRG_1022:g.52345del

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.482-38del MANE Select ENSP00000256958.2:n.482-38del
ENST00000256958.2:c.482-38del ENSP00000256958.2:n.482-38del
NM_006446.4:c.482-38del , LRG_1022t1:c.482-38del NP_006437.3:n.482-38del
NM_006446.5:c.482-38del MANE Select NP_006437.3:n.482-38del
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Search 100 bp 3'