Canonical Allele Identifier: CA535782197

Gene:

Linked Data

• dbSNP Id: rs1366374521
• gnomAD v2: 2-123126781-TA-T
• gnomAD v3: 2-122369205-TA-T
• gnomAD v4: 2-122369205-TA-T
• MyVariant Identifiers: chr2:g.123126782del (hg19) ; chr2:g.122369206del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.122369206del , CM000664.2:g.122369206del	GRCh38
NC_000002.11:g.123126782del , CM000664.1:g.123126782del	GRCh37
NC_000002.10:g.122843252del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_923278.1:n.556-23757del
XR_001739684.1:n.556-23757del