Canonical Allele Identifier: CA2021009517
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1941348863
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21215639del , CM000674.2:g.21215639del GRCh38
NC_000012.11:g.21368573del , CM000674.1:g.21368573del GRCh37
NC_000012.10:g.21259840del NCBI36
NG_011745.1:g.89446del , LRG_1022:g.89446del

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.1498-1480del MANE Select ENSP00000256958.2:n.1498-1480del
ENST00000256958.2:c.1498-1480del ENSP00000256958.2:n.1498-1480del
NM_006446.4:c.1498-1480del , LRG_1022t1:c.1498-1480del NP_006437.3:n.1498-1480del
NM_006446.5:c.1498-1480del MANE Select NP_006437.3:n.1498-1480del
Search 100 bp 5'
Search 100 bp 3'