Canonical Allele Identifier: CA575244605

Gene:

Linked Data

• dbSNP Id: rs577308769
• gnomAD v2: 7-68611784-GT-G
• gnomAD v3: 7-69146797-GT-G
• gnomAD v4: 7-69146797-GT-G
• MyVariant Identifiers: chr7:g.68611785del (hg19) ; chr7:g.69146798del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.69146807del , CM000669.2:g.69146807del	GRCh38
NC_000007.13:g.68611794del , CM000669.1:g.68611794del	GRCh37
NC_000007.12:g.68249730del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_927647.1:n.88-672del