Canonical Allele Identifier: CA212317621
Gene: CNNM2 HGNC NCBI

Linked Data

dbSNP Id: rs893078648

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.103086352A>G , CM000672.2:g.103086352A>G GRCh38
NC_000010.10:g.104846109A>G , CM000672.1:g.104846109A>G GRCh37
NC_000010.9:g.104836099A>G NCBI36
NG_042272.1:g.111955T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000369878.9:c.*9172A>G MANE Select ENSP00000358894.3:n.*9172A>G
ENST00000369878.8:c.*9172A>G ENSP00000358894.3:n.*9172A>G
XR_001747118.1:n.12053A>G
XR_001747121.1:n.12017A>G
NM_017649.5:c.*9172A>G MANE Select NP_060119.3:n.*9172A>G
NM_199076.3:c.*9172A>G NP_951058.1:n.*9172A>G