Canonical Allele Identifier: CA2610736869
Gene: CNNM2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.103086449A>T , CM000672.2:g.103086449A>T GRCh38
NC_000010.10:g.104846206A>T , CM000672.1:g.104846206A>T GRCh37
NC_000010.9:g.104836196A>T NCBI36
NG_042272.1:g.111858T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369878.9:c.*9269A>T MANE Select ENSP00000358894.3:n.*9269A>T
ENST00000369878.8:c.*9269A>T ENSP00000358894.3:n.*9269A>T
XR_001747118.1:n.12150A>T
XR_001747121.1:n.12114A>T
NM_017649.5:c.*9269A>T MANE Select NP_060119.3:n.*9269A>T
NM_199076.3:c.*9269A>T NP_951058.1:n.*9269A>T