Canonical Allele Identifier: CA2020990532
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1940824197

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21176612C>G , CM000674.2:g.21176612C>G GRCh38
NC_000012.11:g.21329546C>G , CM000674.1:g.21329546C>G GRCh37
NC_000012.10:g.21220813C>G NCBI36
NG_011745.1:g.50419C>G , LRG_1022:g.50419C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.360-164C>G MANE Select ENSP00000256958.2:n.360-164C>G
ENST00000256958.2:c.360-164C>G ENSP00000256958.2:n.360-164C>G
ENST00000543498.5:c.426-164C>G
NM_006446.4:c.360-164C>G , LRG_1022t1:c.360-164C>G NP_006437.3:n.360-164C>G
NM_006446.5:c.360-164C>G MANE Select NP_006437.3:n.360-164C>G