Canonical Allele Identifier: CA803406426

Gene:

Linked Data

• dbSNP Id: rs1224895589
• gnomAD v3: 5-126002843-G-A
• gnomAD v4: 5-126002843-G-A
• MyVariant Identifiers: chr5:g.125338536G>A (hg19) ; chr5:g.126002843G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.126002843G>A , CM000667.2:g.126002843G>A	GRCh38
NC_000005.9:g.125338536G>A , CM000667.1:g.125338536G>A	GRCh37
NC_000005.8:g.125366435G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_948737.1:n.565+3497C>T
XR_948738.1:n.497+5697C>T