Canonical Allele Identifier: CA2021001461
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1941146674

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21200633del , CM000674.2:g.21200633del GRCh38
NC_000012.11:g.21353567del , CM000674.1:g.21353567del GRCh37
NC_000012.10:g.21244834del NCBI36
NG_011745.1:g.74440del , LRG_1022:g.74440del

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.1096del MANE Select ENSP00000256958.2:p.Gln366SerfsTer16
ENST00000256958.2:c.1096del ENSP00000256958.2:p.Gln366SerfsTer16
NM_006446.4:c.1096del , LRG_1022t1:c.1096del NP_006437.3:p.Gln366SerfsTer16
NM_006446.5:c.1096del MANE Select NP_006437.3:p.Gln366SerfsTer16