Canonical Allele Identifier: CA2610736806
Gene: CNNM2 HGNC NCBI

Linked Data

gnomAD v4: 10-103086372-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.103086372C>T , CM000672.2:g.103086372C>T GRCh38
NC_000010.10:g.104846129C>T , CM000672.1:g.104846129C>T GRCh37
NC_000010.9:g.104836119C>T NCBI36
NG_042272.1:g.111935G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369878.9:c.*9192C>T MANE Select ENSP00000358894.3:n.*9192C>T
ENST00000369878.8:c.*9192C>T ENSP00000358894.3:n.*9192C>T
XR_001747118.1:n.12073C>T
XR_001747121.1:n.12037C>T
NM_017649.5:c.*9192C>T MANE Select NP_060119.3:n.*9192C>T
NM_199076.3:c.*9192C>T NP_951058.1:n.*9192C>T
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