Canonical Allele Identifier: CA54579238

Gene:

Linked Data

• dbSNP Id: rs756435696
• gnomAD v3: 2-118079596-G-A
• gnomAD v4: 2-118079596-G-A
• MyVariant Identifiers: chr2:g.118837172G>A (hg19) ; chr2:g.118079596G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.118079596G>A , CM000664.2:g.118079596G>A	GRCh38
NC_000002.11:g.118837172G>A , CM000664.1:g.118837172G>A	GRCh37
NC_000002.10:g.118553642G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011512305.1:c.697-2064C>T	XP_011510607.1:n.697-2064C>T
XR_001739662.2:n.138+8655C>T