Canonical Allele Identifier: CA686380280
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1161914923
gnomAD v3: 12-21215617-AT-A
gnomAD v4: 12-21215617-AT-A
MyVariant Identifiers: chr12:g.21368552del (hg19) chr12:g.21215618del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21215618del , CM000674.2:g.21215618del GRCh38
NC_000012.11:g.21368552del , CM000674.1:g.21368552del GRCh37
NC_000012.10:g.21259819del NCBI36
NG_011745.1:g.89425del , LRG_1022:g.89425del

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.1498-1501del MANE Select ENSP00000256958.2:n.1498-1501del
ENST00000256958.2:c.1498-1501del ENSP00000256958.2:n.1498-1501del
NM_006446.4:c.1498-1501del , LRG_1022t1:c.1498-1501del NP_006437.3:n.1498-1501del
NM_006446.5:c.1498-1501del MANE Select NP_006437.3:n.1498-1501del
Search 100 bp 5'
Search 100 bp 3'