Canonical Allele Identifier: CA841571693

Gene:

Linked Data

• dbSNP Id: rs1228892447
• gnomAD v3: 7-69146938-CT-C
• gnomAD v4: 7-69146938-CT-C
• MyVariant Identifiers: chr7:g.68611926del (hg19) ; chr7:g.69146939del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.69146941del , CM000669.2:g.69146941del	GRCh38
NC_000007.13:g.68611928del , CM000669.1:g.68611928del	GRCh37
NC_000007.12:g.68249864del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_927647.1:n.88-813del