Canonical Allele Identifier: CA680801378

Gene:

Linked Data

• dbSNP Id: rs1454715655
• MyVariant Identifiers: chr11:g.80562660_80562663del (hg19) ; chr11:g.80851617_80851620del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.80851619_80851622del , CM000673.2:g.80851619_80851622del	GRCh38
NC_000011.9:g.80562662_80562665del , CM000673.1:g.80562662_80562665del	GRCh37
NC_000011.8:g.80240310_80240313del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_247272.2:n.124+60671_124+60674del