Canonical Allele Identifier: CA6476711
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs752212835
ExAC: 12:21331495 CTCTTA / C
gnomAD v2: 12-21331495-CTCTTA-C
gnomAD v3: 12-21178561-CTCTTA-C
gnomAD v4: 12-21178561-CTCTTA-C
MyVariant Identifiers: chr12:g.21331496_21331500del (hg19) chr12:g.21178562_21178566del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21178565_21178569del , CM000674.2:g.21178565_21178569del GRCh38
NC_000012.11:g.21331499_21331503del , CM000674.1:g.21331499_21331503del GRCh37
NC_000012.10:g.21222766_21222770del NCBI36
NG_011745.1:g.52372_52376del , LRG_1022:g.52372_52376del

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.482-11_482-7del MANE Select ENSP00000256958.2:n.482-11_482-7del
ENST00000256958.2:c.482-11_482-7del ENSP00000256958.2:n.482-11_482-7del
NM_006446.4:c.482-11_482-7del , LRG_1022t1:c.482-11_482-7del NP_006437.3:n.482-11_482-7del
NM_006446.5:c.482-11_482-7del MANE Select NP_006437.3:n.482-11_482-7del
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