Canonical Allele Identifier: CA233565620
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs370967766

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21215714C>G , CM000674.2:g.21215714C>G GRCh38
NC_000012.11:g.21368648C>G , CM000674.1:g.21368648C>G GRCh37
NC_000012.10:g.21259915C>G NCBI36
NG_011745.1:g.89521C>G , LRG_1022:g.89521C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.1498-1405C>G MANE Select ENSP00000256958.2:n.1498-1405C>G
ENST00000256958.2:c.1498-1405C>G ENSP00000256958.2:n.1498-1405C>G
NM_006446.4:c.1498-1405C>G , LRG_1022t1:c.1498-1405C>G NP_006437.3:n.1498-1405C>G
NM_006446.5:c.1498-1405C>G MANE Select NP_006437.3:n.1498-1405C>G