Canonical Allele Identifier: CA1932995590
Gene: CNNM2 HGNC NCBI

Linked Data

dbSNP Id: rs2065812197

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.103086421dup , CM000672.2:g.103086421dup GRCh38
NC_000010.10:g.104846178dup , CM000672.1:g.104846178dup GRCh37
NC_000010.9:g.104836168dup NCBI36
NG_042272.1:g.111886dup

Transcript Alleles

HGVS Amino-acid change
ENST00000369878.9:c.*9241dup MANE Select ENSP00000358894.3:n.*9241dup
ENST00000369878.8:c.*9241dup ENSP00000358894.3:n.*9241dup
XR_001747118.1:n.12122dup
XR_001747121.1:n.12086dup
NM_017649.5:c.*9241dup MANE Select NP_060119.3:n.*9241dup
NM_199076.3:c.*9241dup NP_951058.1:n.*9241dup