Canonical Allele Identifier: CA233565691
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1024296798

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21215740A>C , CM000674.2:g.21215740A>C GRCh38
NC_000012.11:g.21368674A>C , CM000674.1:g.21368674A>C GRCh37
NC_000012.10:g.21259941A>C NCBI36
NG_011745.1:g.89547A>C , LRG_1022:g.89547A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.1498-1379A>C MANE Select ENSP00000256958.2:n.1498-1379A>C
ENST00000256958.2:c.1498-1379A>C ENSP00000256958.2:n.1498-1379A>C
NM_006446.4:c.1498-1379A>C , LRG_1022t1:c.1498-1379A>C NP_006437.3:n.1498-1379A>C
NM_006446.5:c.1498-1379A>C MANE Select NP_006437.3:n.1498-1379A>C