Canonical Allele Identifier: CA16410439

Gene:

Linked Data

• dbSNP Id: rs10500784
• gnomAD v2: 11-13573825-A-C
• gnomAD v3: 11-13552278-A-C
• gnomAD v4: 11-13552278-A-C
• MyVariant Identifiers: chr11:g.13573825A>C (hg19) ; chr11:g.13552278A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.13552278A>C , CM000673.2:g.13552278A>C	GRCh38
NC_000011.9:g.13573825A>C , CM000673.1:g.13573825A>C	GRCh37
NC_000011.8:g.13530401A>C	NCBI36