Canonical Allele Identifier: CA15644698

Gene: CNNM2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102988961A>G , CM000672.2:g.102988961A>G	GRCh38
NC_000010.10:g.104748718A>G , CM000672.1:g.104748718A>G	GRCh37
NC_000010.9:g.104738708A>G	NCBI36
NG_031932.1:g.75644A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369878.9:c.1622-60746A>G MANE Select	ENSP00000358894.3:n.1622-60746A>G
ENST00000369878.8:c.1622-60746A>G	ENSP00000358894.3:n.1622-60746A>G
ENST00000433628.2:c.1622-60746A>G	ENSP00000392875.2:n.1622-60746A>G
NM_017649.4:c.1622-60746A>G	NP_060119.3:n.1622-60746A>G
NM_199076.2:c.1622-60746A>G	NP_951058.1:n.1622-60746A>G
XR_945780.1:n.1810-60746A>G
XR_945781.1:n.1810-38404A>G
XR_945782.1:n.1810-38404A>G
XR_001747118.1:n.1810-60746A>G
XR_001747119.2:n.1810-60746A>G
XR_001747121.1:n.1810-38404A>G
XR_945782.3:n.1810-38404A>G
NM_017649.5:c.1622-60746A>G MANE Select	NP_060119.3:n.1622-60746A>G
NM_199076.3:c.1622-60746A>G	NP_951058.1:n.1622-60746A>G