Canonical Allele Identifier: CA686367895
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1478028774
gnomAD v3: 12-21200868-TC-T
gnomAD v4: 12-21200868-TC-T
MyVariant Identifiers: chr12:g.21353803del (hg19) chr12:g.21200869del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21200869del , CM000674.2:g.21200869del GRCh38
NC_000012.11:g.21353803del , CM000674.1:g.21353803del GRCh37
NC_000012.10:g.21245070del NCBI36
NG_011745.1:g.74676del , LRG_1022:g.74676del

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.1135+197del MANE Select ENSP00000256958.2:n.1135+197del
ENST00000256958.2:c.1135+197del ENSP00000256958.2:n.1135+197del
NM_006446.4:c.1135+197del , LRG_1022t1:c.1135+197del NP_006437.3:n.1135+197del
NM_006446.5:c.1135+197del MANE Select NP_006437.3:n.1135+197del
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Search 100 bp 3'