Canonical Allele Identifier: CA12780435

Gene:

Linked Data

• ClinVar Variation Id: 759405
• ClinVar RCV Id: RCV000937219
• dbSNP Id: rs1799998
• gnomAD v2: 8-143999600-A-G
• gnomAD v3: 8-142918184-A-G
• gnomAD v4: 8-142918184-A-G
• MyVariant Identifiers: chr8:g.143999600A>G (hg19) ; chr8:g.142918184A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.142918184A>G , CM000670.2:g.142918184A>G	GRCh38
NC_000008.10:g.143999600A>G , CM000670.1:g.143999600A>G	GRCh37
NC_000008.9:g.143996602A>G	NCBI36
NG_008374.1:g.4660T>C