Canonical Allele Identifier: CA1375227703

Gene: CNTN3

Linked Data

• dbSNP Id: rs1704454452

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.74578608A>G , CM000665.2:g.74578608A>G	GRCh38
NC_000003.11:g.74627759A>G , CM000665.1:g.74627759A>G	GRCh37
NC_000003.10:g.74710449A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000263665.7:c.-81+35783T>C MANE Select	ENSP00000263665.6:n.-81+35783T>C
XM_005264757.2:c.-81+35783T>C	XP_005264814.1:n.-81+35783T>C
XM_005264758.2:c.-81+35783T>C	XP_005264815.1:n.-81+35783T>C
XM_005264757.3:c.-81+35783T>C	XP_005264814.1:n.-81+35783T>C
XM_017006507.1:c.-81+35140T>C	XP_016861996.1:n.-81+35140T>C
NM_001393376.1:c.-81+35140T>C	NP_001380305.1:n.-81+35140T>C
NM_020872.3:c.-81+35783T>C MANE Select	NP_065923.1:n.-81+35783T>C