Canonical Allele Identifier: CA1932995571
Gene: CNNM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.103086370A= , CM000672.2:g.103086370A= GRCh38
NC_000010.10:g.104846127A= , CM000672.1:g.104846127A= GRCh37
NC_000010.9:g.104836117A= NCBI36
NG_042272.1:g.111937T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369878.9:c.*9190A= MANE Select ENSP00000358894.3:n.*9190A=
ENST00000369878.8:c.*9190A= ENSP00000358894.3:n.*9190A=
XR_001747118.1:n.12071A=
XR_001747121.1:n.12035A=
NM_017649.5:c.*9190A= MANE Select NP_060119.3:n.*9190A=
NM_199076.3:c.*9190A= NP_951058.1:n.*9190A=