Canonical Allele Identifier: CA259811
Gene: SLCO1B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 30439
dbSNP Id: rs183501729

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21196975C>T , CM000674.2:g.21196975C>T GRCh38
NC_000012.11:g.21349909C>T , CM000674.1:g.21349909C>T GRCh37
NC_000012.10:g.21241176C>T NCBI36
NG_011745.1:g.70782C>T , LRG_1022:g.70782C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.757C>T MANE Select ENSP00000256958.2:p.Arg253Ter
ENST00000256958.2:c.757C>T ENSP00000256958.2:p.Arg253Ter
NM_006446.4:c.757C>T , LRG_1022t1:c.757C>T NP_006437.3:p.Arg253Ter
NM_006446.5:c.757C>T MANE Select NP_006437.3:p.Arg253Ter