Canonical Allele Identifier: CA1375227686

Gene: CNTN3

Linked Data

• dbSNP Id: rs1704453952

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.74578569G>T , CM000665.2:g.74578569G>T	GRCh38
NC_000003.11:g.74627720G>T , CM000665.1:g.74627720G>T	GRCh37
NC_000003.10:g.74710410G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000263665.7:c.-81+35822C>A MANE Select	ENSP00000263665.6:n.-81+35822C>A
XM_005264757.2:c.-81+35822C>A	XP_005264814.1:n.-81+35822C>A
XM_005264758.2:c.-81+35822C>A	XP_005264815.1:n.-81+35822C>A
XM_005264757.3:c.-81+35822C>A	XP_005264814.1:n.-81+35822C>A
XM_017006507.1:c.-81+35179C>A	XP_016861996.1:n.-81+35179C>A
NM_001393376.1:c.-81+35179C>A	NP_001380305.1:n.-81+35179C>A
NM_020872.3:c.-81+35822C>A MANE Select	NP_065923.1:n.-81+35822C>A