Canonical Allele Identifier: CA2021009583
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1941350445
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21215773del , CM000674.2:g.21215773del GRCh38
NC_000012.11:g.21368707del , CM000674.1:g.21368707del GRCh37
NC_000012.10:g.21259974del NCBI36
NG_011745.1:g.89580del , LRG_1022:g.89580del

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.1498-1346del MANE Select ENSP00000256958.2:n.1498-1346del
ENST00000256958.2:c.1498-1346del ENSP00000256958.2:n.1498-1346del
NM_006446.4:c.1498-1346del , LRG_1022t1:c.1498-1346del NP_006437.3:n.1498-1346del
NM_006446.5:c.1498-1346del MANE Select NP_006437.3:n.1498-1346del
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