Canonical Allele Identifier: CA2021009393
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1941345843

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21215400_21215402del , CM000674.2:g.21215400_21215402del GRCh38
NC_000012.11:g.21368334_21368336del , CM000674.1:g.21368334_21368336del GRCh37
NC_000012.10:g.21259601_21259603del NCBI36
NG_011745.1:g.89207_89209del , LRG_1022:g.89207_89209del

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.1498-1719_1498-1717del MANE Select ENSP00000256958.2:n.1498-1719_1498-1717del
ENST00000256958.2:c.1498-1719_1498-1717del ENSP00000256958.2:n.1498-1719_1498-1717del
NM_006446.4:c.1498-1719_1498-1717del , LRG_1022t1:c.1498-1719_1498-1717del NP_006437.3:n.1498-1719_1498-1717del
NM_006446.5:c.1498-1719_1498-1717del MANE Select NP_006437.3:n.1498-1719_1498-1717del