Canonical Allele Identifier: CA1932995531

Gene: CNNM2

Linked Data

• dbSNP Id: rs2065809346

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.103086314del , CM000672.2:g.103086314del	GRCh38
NC_000010.10:g.104846071del , CM000672.1:g.104846071del	GRCh37
NC_000010.9:g.104836061del	NCBI36
NG_042272.1:g.111993del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369878.9:c.*9134del MANE Select	ENSP00000358894.3:n.*9134del
ENST00000369878.8:c.*9134del	ENSP00000358894.3:n.*9134del
XR_001747118.1:n.12015del
XR_001747121.1:n.11979del
NM_017649.5:c.*9134del MANE Select	NP_060119.3:n.*9134del
NM_199076.3:c.*9134del	NP_951058.1:n.*9134del