Canonical Allele Identifier: CA124924620

Gene:

Linked Data

• ClinVar Variation Id: 537693
• ClinVar RCV Id: RCV003767872
• dbSNP Id: rs571137741
• gnomAD v3: 5-112707394-A-G
• gnomAD v4: 5-112707394-A-G
• MyVariant Identifiers: chr5:g.112043091A>G (hg19) ; chr5:g.112707394A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707394A>G , CM000667.2:g.112707394A>G	GRCh38
NC_000005.9:g.112043091A>G , CM000667.1:g.112043091A>G	GRCh37
NC_000005.8:g.112070990A>G	NCBI36
NG_008481.4:g.19874A>G , LRG_130:g.19874A>G