Canonical Allele Identifier: CA659071184
Gene: CNNM2 HGNC NCBI

Linked Data

dbSNP Id: rs1331812473
MyVariant Identifiers: chr10:g.104845990del (hg19) chr10:g.103086233del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.103086237del , CM000672.2:g.103086237del GRCh38
NC_000010.10:g.104845994del , CM000672.1:g.104845994del GRCh37
NC_000010.9:g.104835984del NCBI36
NG_042272.1:g.112074del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369878.9:c.*9057del MANE Select ENSP00000358894.3:n.*9057del
ENST00000369878.8:c.*9057del ENSP00000358894.3:n.*9057del
XR_001747118.1:n.11938del
XR_001747121.1:n.11902del
NM_017649.5:c.*9057del MANE Select NP_060119.3:n.*9057del
NM_199076.3:c.*9057del NP_951058.1:n.*9057del
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