Canonical Allele Identifier: CA478863887
Gene: SLCO1B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.21349932T>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21196998T>C , CM000674.2:g.21196998T>C GRCh38
NC_000012.11:g.21349932T>C , CM000674.1:g.21349932T>C GRCh37
NC_000012.10:g.21241199T>C NCBI36
NG_011745.1:g.70805T>C , LRG_1022:g.70805T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.780T>C MANE Select ENSP00000256958.2:p.Leu260=
ENST00000256958.2:c.780T>C ENSP00000256958.2:p.Leu260=
NM_006446.4:c.780T>C , LRG_1022t1:c.780T>C NP_006437.3:p.Leu260=
NM_006446.5:c.780T>C MANE Select NP_006437.3:p.Leu260=
Search 100 bp 5'
Search 100 bp 3'