Canonical Allele Identifier: CA297930301

Gene: CDH2

Linked Data

• dbSNP Id: rs187731393
• gnomAD v3: 18-28120767-T-G
• gnomAD v4: 18-28120767-T-G
• MyVariant Identifiers: chr18:g.25700731T>G (hg19) ; chr18:g.28120767T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.28120767T>G , CM000680.2:g.28120767T>G	GRCh38
NC_000018.9:g.25700731T>G , CM000680.1:g.25700731T>G	GRCh37
NC_000018.8:g.23954729T>G	NCBI36
NG_011959.1:g.61715A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269141.8:c.172+26906A>C MANE Select	ENSP00000269141.3:n.172+26906A>C
ENST00000413878.2:c.-84+26906A>C	ENSP00000414269.2:n.-84+26906A>C
ENST00000430882.6:c.-275-23513A>C	ENSP00000412120.2:n.-275-23513A>C
ENST00000675708.1:c.-84+26906A>C	ENSP00000501654.1:n.-84+26906A>C
ENST00000676445.1:c.-84+26906A>C	ENSP00000502206.1:n.-84+26906A>C
ENST00000269141.7:c.172+26906A>C	ENSP00000269141.3:n.172+26906A>C
ENST00000413878.1:c.-84+26906A>C	ENSP00000414269.1:n.-84+26906A>C
NM_001792.3:c.172+26906A>C	NP_001783.2:n.172+26906A>C
NM_001792.4:c.172+26906A>C	NP_001783.2:n.172+26906A>C
XM_005258181.2:c.118+26906A>C	XP_005258238.1:n.118+26906A>C
XM_011525787.1:c.118+26906A>C	XP_011524089.1:n.118+26906A>C
XM_011525788.1:c.-84+26906A>C	XP_011524090.1:n.-84+26906A>C
XM_017025514.2:c.172+26906A>C	XP_016881003.1:n.172+26906A>C
NM_001792.5:c.172+26906A>C MANE Select	NP_001783.2:n.172+26906A>C