Canonical Allele Identifier: CA1932995641

Gene: CNNM2

Linked Data

• dbSNP Id: rs2065814353

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.103086540_103086541del , CM000672.2:g.103086540_103086541del	GRCh38
NC_000010.10:g.104846297_104846298del , CM000672.1:g.104846297_104846298del	GRCh37
NC_000010.9:g.104836287_104836288del	NCBI36
NG_042272.1:g.111766_111767del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369878.9:c.*9360_*9361del MANE Select	ENSP00000358894.3:n.*9360_*9361del
ENST00000369878.8:c.*9360_*9361del	ENSP00000358894.3:n.*9360_*9361del
XR_001747118.1:n.12241_12242del
XR_001747121.1:n.12205_12206del
NM_017649.5:c.*9360_*9361del MANE Select	NP_060119.3:n.*9360_*9361del
NM_199076.3:c.*9360_*9361del	NP_951058.1:n.*9360_*9361del