Canonical Allele Identifier: CA1375227683
Gene: CNTN3 HGNC NCBI

Linked Data

dbSNP Id: rs1704453887
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.74578566T>C , CM000665.2:g.74578566T>C GRCh38
NC_000003.11:g.74627717T>C , CM000665.1:g.74627717T>C GRCh37
NC_000003.10:g.74710407T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000263665.7:c.-81+35825A>G MANE Select ENSP00000263665.6:n.-81+35825A>G
XM_005264757.2:c.-81+35825A>G XP_005264814.1:n.-81+35825A>G
XM_005264758.2:c.-81+35825A>G XP_005264815.1:n.-81+35825A>G
XM_005264757.3:c.-81+35825A>G XP_005264814.1:n.-81+35825A>G
XM_017006507.1:c.-81+35182A>G XP_016861996.1:n.-81+35182A>G
NM_001393376.1:c.-81+35182A>G NP_001380305.1:n.-81+35182A>G
NM_020872.3:c.-81+35825A>G MANE Select NP_065923.1:n.-81+35825A>G
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