Canonical Allele Identifier: CA10654640

Gene:

Linked Data

• ClinVar Variation Id: 369360
• ClinVar RCV Id: RCV000317743 ; RCV002285326
• dbSNP Id: rs17878855
• gnomAD v2: 21-33031927-G-C
• gnomAD v3: 21-31659614-G-C
• gnomAD v4: 21-31659614-G-C
• MyVariant Identifiers: chr21:g.33031927G>C (hg19) ; chr21:g.31659614G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.31659614G>C , CM000683.2:g.31659614G>C	GRCh38
NC_000021.8:g.33031927G>C , CM000683.1:g.33031927G>C	GRCh37
NC_000021.7:g.31953798G>C	NCBI36
NG_008689.1:g.4993G>C , LRG_652:g.4993G>C