Canonical Allele Identifier: CA77538398

Gene: CNTN3

Linked Data

• dbSNP Id: rs904704131
• gnomAD v3: 3-74578590-G-A
• gnomAD v4: 3-74578590-G-A
• MyVariant Identifiers: chr3:g.74627741G>A (hg19) ; chr3:g.74578590G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.74578590G>A , CM000665.2:g.74578590G>A	GRCh38
NC_000003.11:g.74627741G>A , CM000665.1:g.74627741G>A	GRCh37
NC_000003.10:g.74710431G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263665.7:c.-81+35801C>T MANE Select	ENSP00000263665.6:n.-81+35801C>T
XM_005264757.2:c.-81+35801C>T	XP_005264814.1:n.-81+35801C>T
XM_005264758.2:c.-81+35801C>T	XP_005264815.1:n.-81+35801C>T
XM_005264757.3:c.-81+35801C>T	XP_005264814.1:n.-81+35801C>T
XM_017006507.1:c.-81+35158C>T	XP_016861996.1:n.-81+35158C>T
NM_001393376.1:c.-81+35158C>T	NP_001380305.1:n.-81+35158C>T
NM_020872.3:c.-81+35801C>T MANE Select	NP_065923.1:n.-81+35801C>T