Canonical Allele Identifier: CA2021009325
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1941344664

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21215268_21215270del , CM000674.2:g.21215268_21215270del GRCh38
NC_000012.11:g.21368202_21368204del , CM000674.1:g.21368202_21368204del GRCh37
NC_000012.10:g.21259469_21259471del NCBI36
NG_011745.1:g.89075_89077del , LRG_1022:g.89075_89077del

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.1498-1851_1498-1849del MANE Select ENSP00000256958.2:n.1498-1851_1498-1849del
ENST00000256958.2:c.1498-1851_1498-1849del ENSP00000256958.2:n.1498-1851_1498-1849del
NM_006446.4:c.1498-1851_1498-1849del , LRG_1022t1:c.1498-1851_1498-1849del NP_006437.3:n.1498-1851_1498-1849del
NM_006446.5:c.1498-1851_1498-1849del MANE Select NP_006437.3:n.1498-1851_1498-1849del