Canonical Allele Identifier: CA478866929
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1385183901

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21176881T>G , CM000674.2:g.21176881T>G GRCh38
NC_000012.11:g.21329815T>G , CM000674.1:g.21329815T>G GRCh37
NC_000012.10:g.21221082T>G NCBI36
NG_011745.1:g.50688T>G , LRG_1022:g.50688T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.465T>G MANE Select ENSP00000256958.2:p.Pro155=
ENST00000256958.2:c.465T>G ENSP00000256958.2:p.Pro155=
ENST00000543498.5:c.531T>G
NM_006446.4:c.465T>G , LRG_1022t1:c.465T>G NP_006437.3:p.Pro155=
NM_006446.5:c.465T>G MANE Select NP_006437.3:p.Pro155=