Canonical Allele Identifier: CA112146132

Gene:

Linked Data

• ClinVar Variation Id: 991952
• ClinVar RCV Id: RCV001280253
• dbSNP Id: rs960799140
• gnomAD v3: 4-186265838-A-G
• gnomAD v4: 4-186265838-A-G
• MyVariant Identifiers: chr4:g.187186992A>G (hg19) ; chr4:g.186265838A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186265838A>G , CM000666.2:g.186265838A>G	GRCh38
NC_000004.11:g.187186992A>G , CM000666.1:g.187186992A>G	GRCh37
NC_000004.10:g.187423986A>G	NCBI36
NG_008051.1:g.4875A>G , LRG_583:g.4875A>G