Canonical Allele Identifier: CA2020989810
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1940802582

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21175034C>A , CM000674.2:g.21175034C>A GRCh38
NC_000012.11:g.21327968C>A , CM000674.1:g.21327968C>A GRCh37
NC_000012.10:g.21219235C>A NCBI36
NG_011745.1:g.48841C>A , LRG_1022:g.48841C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.359+325C>A MANE Select ENSP00000256958.2:n.359+325C>A
ENST00000256958.2:c.359+325C>A ENSP00000256958.2:n.359+325C>A
ENST00000543498.5:c.426-1742C>A
NM_006446.4:c.359+325C>A , LRG_1022t1:c.359+325C>A NP_006437.3:n.359+325C>A
NM_006446.5:c.359+325C>A MANE Select NP_006437.3:n.359+325C>A