Canonical Allele Identifier: CA603657579
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1287785294

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21174450A>G , CM000674.2:g.21174450A>G GRCh38
NC_000012.11:g.21327384A>G , CM000674.1:g.21327384A>G GRCh37
NC_000012.10:g.21218651A>G NCBI36
NG_011745.1:g.48257A>G , LRG_1022:g.48257A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.227-127A>G MANE Select ENSP00000256958.2:n.227-127A>G
ENST00000256958.2:c.227-127A>G ENSP00000256958.2:n.227-127A>G
ENST00000543498.5:c.426-2326A>G
NM_006446.4:c.227-127A>G , LRG_1022t1:c.227-127A>G NP_006437.3:n.227-127A>G
NM_006446.5:c.227-127A>G MANE Select NP_006437.3:n.227-127A>G