Canonical Allele Identifier: CA2021009304
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1941344406

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21215225G>C , CM000674.2:g.21215225G>C GRCh38
NC_000012.11:g.21368159G>C , CM000674.1:g.21368159G>C GRCh37
NC_000012.10:g.21259426G>C NCBI36
NG_011745.1:g.89032G>C , LRG_1022:g.89032G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.1498-1894G>C MANE Select ENSP00000256958.2:n.1498-1894G>C
ENST00000256958.2:c.1498-1894G>C ENSP00000256958.2:n.1498-1894G>C
NM_006446.4:c.1498-1894G>C , LRG_1022t1:c.1498-1894G>C NP_006437.3:n.1498-1894G>C
NM_006446.5:c.1498-1894G>C MANE Select NP_006437.3:n.1498-1894G>C