Canonical Allele Identifier: CA2021009682
Gene: SLCO1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21215944_21215947delinsGGAT , CM000674.2:g.21215944_21215947delinsGGAT GRCh38
NC_000012.11:g.21368878_21368881delinsGGAT , CM000674.1:g.21368878_21368881delinsGGAT GRCh37
NC_000012.10:g.21260145_21260148delinsGGAT NCBI36
NG_011745.1:g.89751_89754delinsGGAT , LRG_1022:g.89751_89754delinsGGAT

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.1498-1175_1498-1172delinsGGAT MANE Select ENSP00000256958.2:n.1498-1175_1498-1172delinsGGAT
ENST00000256958.2:c.1498-1175_1498-1172delinsGGAT ENSP00000256958.2:n.1498-1175_1498-1172delinsGGAT
NM_006446.4:c.1498-1175_1498-1172delinsGGAT , LRG_1022t1:c.1498-1175_1498-1172delinsGGAT NP_006437.3:n.1498-1175_1498-1172delinsGGAT
NM_006446.5:c.1498-1175_1498-1172delinsGGAT MANE Select NP_006437.3:n.1498-1175_1498-1172delinsGGAT