Canonical Allele Identifier: CA154890289

Gene:

Linked Data

• dbSNP Id: rs1046669488
• gnomAD v2: 7-17997473-CT-C
• gnomAD v3: 7-17957850-CT-C
• gnomAD v4: 7-17957850-CT-C
• MyVariant Identifiers: chr7:g.17997474del (hg19) ; chr7:g.17957851del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17957851del , CM000669.2:g.17957851del	GRCh38
NC_000007.13:g.17997474del , CM000669.1:g.17997474del	GRCh37
NC_000007.12:g.17963999del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_927078.1:n.271-819del