Canonical Allele Identifier: CA212317623
Gene: CNNM2 HGNC NCBI

Linked Data

dbSNP Id: rs191443123
gnomAD v2: 10-104846119-T-A
gnomAD v3: 10-103086362-T-A
gnomAD v4: 10-103086362-T-A
MyVariant Identifiers: chr10:g.104846119T>A (hg19) chr10:g.103086362T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.103086362T>A , CM000672.2:g.103086362T>A GRCh38
NC_000010.10:g.104846119T>A , CM000672.1:g.104846119T>A GRCh37
NC_000010.9:g.104836109T>A NCBI36
NG_042272.1:g.111945A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000369878.9:c.*9182T>A MANE Select ENSP00000358894.3:n.*9182T>A
ENST00000369878.8:c.*9182T>A ENSP00000358894.3:n.*9182T>A
XR_001747118.1:n.12063T>A
XR_001747121.1:n.12027T>A
NM_017649.5:c.*9182T>A MANE Select NP_060119.3:n.*9182T>A
NM_199076.3:c.*9182T>A NP_951058.1:n.*9182T>A
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