Canonical Allele Identifier: CA606429507
Gene:

Linked Data

dbSNP Id: rs1445726496
gnomAD v2: 12-84564016-A-T
gnomAD v3: 12-84170237-A-T
gnomAD v4: 12-84170237-A-T
MyVariant Identifiers: chr12:g.84564016A>T (hg19) chr12:g.84170237A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.84170237A>T , CM000674.2:g.84170237A>T GRCh38
NC_000012.11:g.84564016A>T , CM000674.1:g.84564016A>T GRCh37
NC_000012.10:g.83088147A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001749234.1:n.127+16229T>A
XR_001749235.1:n.127+16229T>A
Search 100 bp 5'
Search 100 bp 3'