Canonical Allele Identifier: CA686352927
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1445328755

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21174557T>C , CM000674.2:g.21174557T>C GRCh38
NC_000012.11:g.21327491T>C , CM000674.1:g.21327491T>C GRCh37
NC_000012.10:g.21218758T>C NCBI36
NG_011745.1:g.48364T>C , LRG_1022:g.48364T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.227-20T>C MANE Select ENSP00000256958.2:n.227-20T>C
ENST00000256958.2:c.227-20T>C ENSP00000256958.2:n.227-20T>C
ENST00000543498.5:c.426-2219T>C
NM_006446.4:c.227-20T>C , LRG_1022t1:c.227-20T>C NP_006437.3:n.227-20T>C
NM_006446.5:c.227-20T>C MANE Select NP_006437.3:n.227-20T>C