Canonical Allele Identifier: CA2021009478
Gene: SLCO1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21215571_21215572delinsCA , CM000674.2:g.21215571_21215572delinsCA GRCh38
NC_000012.11:g.21368505_21368506delinsCA , CM000674.1:g.21368505_21368506delinsCA GRCh37
NC_000012.10:g.21259772_21259773delinsCA NCBI36
NG_011745.1:g.89378_89379delinsCA , LRG_1022:g.89378_89379delinsCA

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.1498-1548_1498-1547delinsCA MANE Select ENSP00000256958.2:n.1498-1548_1498-1547delinsCA
ENST00000256958.2:c.1498-1548_1498-1547delinsCA ENSP00000256958.2:n.1498-1548_1498-1547delinsCA
NM_006446.4:c.1498-1548_1498-1547delinsCA , LRG_1022t1:c.1498-1548_1498-1547delinsCA NP_006437.3:n.1498-1548_1498-1547delinsCA
NM_006446.5:c.1498-1548_1498-1547delinsCA MANE Select NP_006437.3:n.1498-1548_1498-1547delinsCA