Canonical Allele Identifier: CA1932995536
Gene: CNNM2 HGNC NCBI

Linked Data

dbSNP Id: rs1564878456
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.103086320C>G , CM000672.2:g.103086320C>G GRCh38
NC_000010.10:g.104846077C>G , CM000672.1:g.104846077C>G GRCh37
NC_000010.9:g.104836067C>G NCBI36
NG_042272.1:g.111987G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369878.9:c.*9140C>G MANE Select ENSP00000358894.3:n.*9140C>G
ENST00000369878.8:c.*9140C>G ENSP00000358894.3:n.*9140C>G
XR_001747118.1:n.12021C>G
XR_001747121.1:n.11985C>G
NM_017649.5:c.*9140C>G MANE Select NP_060119.3:n.*9140C>G
NM_199076.3:c.*9140C>G NP_951058.1:n.*9140C>G
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