Canonical Allele Identifier: CA1932995598
Gene: CNNM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.103086440C= , CM000672.2:g.103086440C= GRCh38
NC_000010.10:g.104846197C= , CM000672.1:g.104846197C= GRCh37
NC_000010.9:g.104836187C= NCBI36
NG_042272.1:g.111867G=

Transcript Alleles

HGVS Amino-acid change
ENST00000369878.9:c.*9260C= MANE Select ENSP00000358894.3:n.*9260C=
ENST00000369878.8:c.*9260C= ENSP00000358894.3:n.*9260C=
XR_001747118.1:n.12141C=
XR_001747121.1:n.12105C=
NM_017649.5:c.*9260C= MANE Select NP_060119.3:n.*9260C=
NM_199076.3:c.*9260C= NP_951058.1:n.*9260C=