Canonical Allele Identifier: CA2610736926

Gene: CNNM2

Linked Data

• gnomAD v4: 10-103086514-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.103086514C>T , CM000672.2:g.103086514C>T	GRCh38
NC_000010.10:g.104846271C>T , CM000672.1:g.104846271C>T	GRCh37
NC_000010.9:g.104836261C>T	NCBI36
NG_042272.1:g.111793G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369878.9:c.*9334C>T MANE Select	ENSP00000358894.3:n.*9334C>T
ENST00000369878.8:c.*9334C>T	ENSP00000358894.3:n.*9334C>T
XR_001747118.1:n.12215C>T
XR_001747121.1:n.12179C>T
NM_017649.5:c.*9334C>T MANE Select	NP_060119.3:n.*9334C>T
NM_199076.3:c.*9334C>T	NP_951058.1:n.*9334C>T