Canonical Allele Identifier: CA1932995629

Gene: CNNM2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.103086503T= , CM000672.2:g.103086503T=	GRCh38
NC_000010.10:g.104846260T= , CM000672.1:g.104846260T=	GRCh37
NC_000010.9:g.104836250T=	NCBI36
NG_042272.1:g.111804A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369878.9:c.*9323T= MANE Select	ENSP00000358894.3:n.*9323T=
ENST00000369878.8:c.*9323T=	ENSP00000358894.3:n.*9323T=
XR_001747118.1:n.12204T=
XR_001747121.1:n.12168T=
NM_017649.5:c.*9323T= MANE Select	NP_060119.3:n.*9323T=
NM_199076.3:c.*9323T=	NP_951058.1:n.*9323T=