Canonical Allele Identifier: CA2610736795
Gene: CNNM2 HGNC NCBI

Linked Data

gnomAD v4: 10-103086359-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.103086359A>G , CM000672.2:g.103086359A>G GRCh38
NC_000010.10:g.104846116A>G , CM000672.1:g.104846116A>G GRCh37
NC_000010.9:g.104836106A>G NCBI36
NG_042272.1:g.111948T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000369878.9:c.*9179A>G MANE Select ENSP00000358894.3:n.*9179A>G
ENST00000369878.8:c.*9179A>G ENSP00000358894.3:n.*9179A>G
XR_001747118.1:n.12060A>G
XR_001747121.1:n.12024A>G
NM_017649.5:c.*9179A>G MANE Select NP_060119.3:n.*9179A>G
NM_199076.3:c.*9179A>G NP_951058.1:n.*9179A>G
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