Canonical Allele Identifier: CA672220118

Gene:

Linked Data

• dbSNP Id: rs1183557015
• MyVariant Identifiers: chr11:g.116313469_116313475del (hg19) ; chr11:g.116442752_116442758del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116442753_116442759del , CM000673.2:g.116442753_116442759del	GRCh38
NC_000011.9:g.116313470_116313476del , CM000673.1:g.116313470_116313476del	GRCh37
NC_000011.8:g.115818680_115818686del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001748403.1:n.349+31119_349+31125del