Canonical Allele Identifier: CA233565607
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1036130423
MyVariant Identifiers: chr12:g.21368644G>A (hg19) chr12:g.21215710G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21215710G>A , CM000674.2:g.21215710G>A GRCh38
NC_000012.11:g.21368644G>A , CM000674.1:g.21368644G>A GRCh37
NC_000012.10:g.21259911G>A NCBI36
NG_011745.1:g.89517G>A , LRG_1022:g.89517G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.1498-1409G>A MANE Select ENSP00000256958.2:n.1498-1409G>A
ENST00000256958.2:c.1498-1409G>A ENSP00000256958.2:n.1498-1409G>A
NM_006446.4:c.1498-1409G>A , LRG_1022t1:c.1498-1409G>A NP_006437.3:n.1498-1409G>A
NM_006446.5:c.1498-1409G>A MANE Select NP_006437.3:n.1498-1409G>A
Search 100 bp 5'
Search 100 bp 3'