Canonical Allele Identifier: CA2610736862
Gene: CNNM2 HGNC NCBI

Linked Data

gnomAD v4: 10-103086435-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.103086435C>A , CM000672.2:g.103086435C>A GRCh38
NC_000010.10:g.104846192C>A , CM000672.1:g.104846192C>A GRCh37
NC_000010.9:g.104836182C>A NCBI36
NG_042272.1:g.111872G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000369878.9:c.*9255C>A MANE Select ENSP00000358894.3:n.*9255C>A
ENST00000369878.8:c.*9255C>A ENSP00000358894.3:n.*9255C>A
XR_001747118.1:n.12136C>A
XR_001747121.1:n.12100C>A
NM_017649.5:c.*9255C>A MANE Select NP_060119.3:n.*9255C>A
NM_199076.3:c.*9255C>A NP_951058.1:n.*9255C>A
Search 100 bp 5'
Search 100 bp 3'