Canonical Allele Identifier: CA2020999788
Gene: SLCO1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21196814_21196815delinsCA , CM000674.2:g.21196814_21196815delinsCA GRCh38
NC_000012.11:g.21349748_21349749delinsCA , CM000674.1:g.21349748_21349749delinsCA GRCh37
NC_000012.10:g.21241015_21241016delinsCA NCBI36
NG_011745.1:g.70621_70622delinsCA , LRG_1022:g.70621_70622delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.728-132_728-131delinsCA MANE Select ENSP00000256958.2:n.728-132_728-131delinsCA
ENST00000256958.2:c.728-132_728-131delinsCA ENSP00000256958.2:n.728-132_728-131delinsCA
NM_006446.4:c.728-132_728-131delinsCA , LRG_1022t1:c.728-132_728-131delinsCA NP_006437.3:n.728-132_728-131delinsCA
NM_006446.5:c.728-132_728-131delinsCA MANE Select NP_006437.3:n.728-132_728-131delinsCA