Canonical Allele Identifier: CA1932995601
Gene: CNNM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.103086454A= , CM000672.2:g.103086454A= GRCh38
NC_000010.10:g.104846211A= , CM000672.1:g.104846211A= GRCh37
NC_000010.9:g.104836201A= NCBI36
NG_042272.1:g.111853T=

Transcript Alleles

HGVS Amino-acid change
ENST00000369878.9:c.*9274A= MANE Select ENSP00000358894.3:n.*9274A=
ENST00000369878.8:c.*9274A= ENSP00000358894.3:n.*9274A=
XR_001747118.1:n.12155A=
XR_001747121.1:n.12119A=
NM_017649.5:c.*9274A= MANE Select NP_060119.3:n.*9274A=
NM_199076.3:c.*9274A= NP_951058.1:n.*9274A=