Canonical Allele Identifier: CA836257740

Gene:

Linked Data

• dbSNP Id: rs1473498757
• MyVariant Identifiers: chr7:g.17997481_17997483del (hg19) ; chr7:g.17957858_17957860del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17957861_17957863del , CM000669.2:g.17957861_17957863del	GRCh38
NC_000007.13:g.17997484_17997486del , CM000669.1:g.17997484_17997486del	GRCh37
NC_000007.12:g.17964009_17964011del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_927078.1:n.271-809_271-807del