Canonical Allele Identifier: CA11358693
Gene:

Linked Data

dbSNP Id: rs106871
gnomAD v2: 3-41085459-G-A
gnomAD v3: 3-41043968-G-A
gnomAD v4: 3-41043968-G-A
MyVariant Identifiers: chr3:g.41085459G>A (hg19) chr3:g.41043968G>A (hg38)
Allelic Epigenome: Alellic Epigenome (raw data)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.41043968G>A , CM000665.2:g.41043968G>A GRCh38
NC_000003.11:g.41085459G>A , CM000665.1:g.41085459G>A GRCh37
NC_000003.10:g.41060463G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_940768.1:n.6C>T
Search 100 bp 5'
Search 100 bp 3'