Canonical Allele Identifier: CA2020989794
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1591809006

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21174997A>G , CM000674.2:g.21174997A>G GRCh38
NC_000012.11:g.21327931A>G , CM000674.1:g.21327931A>G GRCh37
NC_000012.10:g.21219198A>G NCBI36
NG_011745.1:g.48804A>G , LRG_1022:g.48804A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.359+288A>G MANE Select ENSP00000256958.2:n.359+288A>G
ENST00000256958.2:c.359+288A>G ENSP00000256958.2:n.359+288A>G
ENST00000543498.5:c.426-1779A>G
NM_006446.4:c.359+288A>G , LRG_1022t1:c.359+288A>G NP_006437.3:n.359+288A>G
NM_006446.5:c.359+288A>G MANE Select NP_006437.3:n.359+288A>G