Canonical Allele Identifier: CA64382919

Gene:

Linked Data

• dbSNP Id: rs34690328
• gnomAD v2: 2-200897976-AATTT-A
• gnomAD v3: 2-200033253-AATTT-A
• gnomAD v4: 2-200033253-AATTT-A
• MyVariant Identifiers: chr2:g.200897977_200897980del (hg19) ; chr2:g.200033254_200033257del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.200033274_200033277del , CM000664.2:g.200033274_200033277del	GRCh38
NC_000002.11:g.200897997_200898000del , CM000664.1:g.200897997_200898000del	GRCh37
NC_000002.10:g.200606242_200606245del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_923778.1:n.178-22361_178-22358del