Canonical Allele Identifier: CA10587124

Gene:

Linked Data

• ClinVar Variation Id: 256342
• ClinVar RCV Id: RCV000247556 ; RCV001594893
• dbSNP Id: rs7110263
• gnomAD v2: 11-5246512-T-G
• gnomAD v3: 11-5225282-T-G
• gnomAD v4: 11-5225282-T-G
• MyVariant Identifiers: chr11:g.5246512T>G (hg19) ; chr11:g.5225282T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5225282T>G , CM000673.2:g.5225282T>G	GRCh38
NC_000011.9:g.5246512T>G , CM000673.1:g.5246512T>G	GRCh37
NC_000011.8:g.5203088T>G	NCBI36
NG_000007.3:g.72334A>C
NG_059281.1:g.6790A>C