Canonical Allele Identifier: CA2020999792
Gene: SLCO1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21196827_21196828delinsGA , CM000674.2:g.21196827_21196828delinsGA GRCh38
NC_000012.11:g.21349761_21349762delinsGA , CM000674.1:g.21349761_21349762delinsGA GRCh37
NC_000012.10:g.21241028_21241029delinsGA NCBI36
NG_011745.1:g.70634_70635delinsGA , LRG_1022:g.70634_70635delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.728-119_728-118delinsGA MANE Select ENSP00000256958.2:n.728-119_728-118delinsGA
ENST00000256958.2:c.728-119_728-118delinsGA ENSP00000256958.2:n.728-119_728-118delinsGA
NM_006446.4:c.728-119_728-118delinsGA , LRG_1022t1:c.728-119_728-118delinsGA NP_006437.3:n.728-119_728-118delinsGA
NM_006446.5:c.728-119_728-118delinsGA MANE Select NP_006437.3:n.728-119_728-118delinsGA