Canonical Allele Identifier: CA384104795
Gene: SLCO1B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21176802T>C , CM000674.2:g.21176802T>C GRCh38
NC_000012.11:g.21329736T>C , CM000674.1:g.21329736T>C GRCh37
NC_000012.10:g.21221003T>C NCBI36
NG_011745.1:g.50609T>C , LRG_1022:g.50609T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.386T>C MANE Select ENSP00000256958.2:p.Ile129Thr
ENST00000256958.2:c.386T>C ENSP00000256958.2:p.Ile129Thr
ENST00000543498.5:c.452T>C
NM_006446.4:c.386T>C , LRG_1022t1:c.386T>C NP_006437.3:p.Ile129Thr
NM_006446.5:c.386T>C MANE Select NP_006437.3:p.Ile129Thr