Canonical Allele Identifier: CA659071327
Gene: CNNM2 HGNC NCBI

Linked Data

dbSNP Id: rs1289040177
MyVariant Identifiers: chr10:g.104846235C>T (hg19) chr10:g.103086478C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.103086478C>T , CM000672.2:g.103086478C>T GRCh38
NC_000010.10:g.104846235C>T , CM000672.1:g.104846235C>T GRCh37
NC_000010.9:g.104836225C>T NCBI36
NG_042272.1:g.111829G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369878.9:c.*9298C>T MANE Select ENSP00000358894.3:n.*9298C>T
ENST00000369878.8:c.*9298C>T ENSP00000358894.3:n.*9298C>T
XR_001747118.1:n.12179C>T
XR_001747121.1:n.12143C>T
NM_017649.5:c.*9298C>T MANE Select NP_060119.3:n.*9298C>T
NM_199076.3:c.*9298C>T NP_951058.1:n.*9298C>T
Search 100 bp 5'
Search 100 bp 3'