Canonical Allele Identifier: CA16095889

Gene:

Linked Data

• dbSNP Id: rs10865170
• gnomAD v2: 2-41761800-C-A
• gnomAD v3: 2-41534660-C-A
• gnomAD v4: 2-41534660-C-A
• MyVariant Identifiers: chr2:g.41761800C>A (hg19) ; chr2:g.41534660C>A (hg38)
• Allelic Epigenome: Alellic Epigenome (raw data)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.41534660C>A , CM000664.2:g.41534660C>A	GRCh38
NC_000002.11:g.41761800C>A , CM000664.1:g.41761800C>A	GRCh37
NC_000002.10:g.41615304C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_939996.1:n.181+3066G>T
XR_939997.1:n.146+3066G>T
XR_939997.2:n.9529+3066G>T