Canonical Allele Identifier: CA679145055

Gene:

Linked Data

• ClinVar Variation Id: 2135980
• ClinVar RCV Id: RCV003313815
• dbSNP Id: rs1800955
• gnomAD v3: 11-636784-T-G
• gnomAD v4: 11-636784-T-G
• MyVariant Identifiers: chr11:g.636784T>G (hg19) ; chr11:g.636784T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.636784T>G , CM000673.2:g.636784T>G	GRCh38
NC_000011.9:g.636784T>G , CM000673.1:g.636784T>G	GRCh37
NC_000011.8:g.626784T>G	NCBI36
NG_021241.1:g.4480T>G