Canonical Allele Identifier: CA112146138

Gene:

Linked Data

• ClinVar Variation Id: 3048113
• ClinVar RCV Id: RCV003951927
• dbSNP Id: rs192994982
• gnomAD v2: 4-187187003-A-G
• gnomAD v3: 4-186265849-A-G
• gnomAD v4: 4-186265849-A-G
• MyVariant Identifiers: chr4:g.187187003A>G (hg19) ; chr4:g.186265849A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186265849A>G , CM000666.2:g.186265849A>G	GRCh38
NC_000004.11:g.187187003A>G , CM000666.1:g.187187003A>G	GRCh37
NC_000004.10:g.187423997A>G	NCBI36
NG_008051.1:g.4886A>G , LRG_583:g.4886A>G