Canonical Allele Identifier: CA2842449128

Gene: CNNM2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.103086412A>G , CM000672.2:g.103086412A>G	GRCh38
NC_000010.10:g.104846169A>G , CM000672.1:g.104846169A>G	GRCh37
NC_000010.9:g.104836159A>G	NCBI36
NG_042272.1:g.111895T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369878.9:c.*9232A>G MANE Select	ENSP00000358894.3:n.*9232A>G
ENST00000369878.8:c.*9232A>G	ENSP00000358894.3:n.*9232A>G
XR_001747118.1:n.12113A>G
XR_001747121.1:n.12077A>G
NM_017649.5:c.*9232A>G MANE Select	NP_060119.3:n.*9232A>G
NM_199076.3:c.*9232A>G	NP_951058.1:n.*9232A>G