Canonical Allele Identifier: CA384105502
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs4149056
MyVariant Identifiers: chr12:g.21331549T>A (hg19) chr12:g.21178615T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21178615T>A , CM000674.2:g.21178615T>A GRCh38
NC_000012.11:g.21331549T>A , CM000674.1:g.21331549T>A GRCh37
NC_000012.10:g.21222816T>A NCBI36
NG_011745.1:g.52422T>A , LRG_1022:g.52422T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.521T>A MANE Select ENSP00000256958.2:p.Val174Glu
ENST00000256958.2:c.521T>A ENSP00000256958.2:p.Val174Glu
NM_006446.4:c.521T>A , LRG_1022t1:c.521T>A NP_006437.3:p.Val174Glu
NM_006446.5:c.521T>A MANE Select NP_006437.3:p.Val174Glu
Search 100 bp 5'
Search 100 bp 3'