Canonical Allele Identifier: CA659071252
Gene: CNNM2 HGNC NCBI

Linked Data

dbSNP Id: rs1367122071
gnomAD v3: 10-103086345-G-A
gnomAD v4: 10-103086345-G-A
MyVariant Identifiers: chr10:g.104846102G>A (hg19) chr10:g.103086345G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.103086345G>A , CM000672.2:g.103086345G>A GRCh38
NC_000010.10:g.104846102G>A , CM000672.1:g.104846102G>A GRCh37
NC_000010.9:g.104836092G>A NCBI36
NG_042272.1:g.111962C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000369878.9:c.*9165G>A MANE Select ENSP00000358894.3:n.*9165G>A
ENST00000369878.8:c.*9165G>A ENSP00000358894.3:n.*9165G>A
XR_001747118.1:n.12046G>A
XR_001747121.1:n.12010G>A
NM_017649.5:c.*9165G>A MANE Select NP_060119.3:n.*9165G>A
NM_199076.3:c.*9165G>A NP_951058.1:n.*9165G>A
Search 100 bp 5'
Search 100 bp 3'