Canonical Allele Identifier: CA63970346

Gene:

Linked Data

• dbSNP Id: rs992510597
• gnomAD v2: 2-204983502-C-CTG
• gnomAD v3: 2-204118779-C-CTG
• gnomAD v4: 2-204118779-C-CTG
• MyVariant Identifiers: chr2:g.204983504_204983505insTG (hg19) ; chr2:g.204983502_204983503insTG (hg19) ; chr2:g.204118781_204118782insTG (hg38) ; chr2:g.204118779_204118780insTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.204118793_204118794dup , CM000664.2:g.204118793_204118794dup	GRCh38
NC_000002.11:g.204983516_204983517dup , CM000664.1:g.204983516_204983517dup	GRCh37
NC_000002.10:g.204691761_204691762dup	NCBI36