Canonical Allele Identifier: CA2600123126
Gene: CNTN3 HGNC NCBI

Linked Data

dbSNP Id: rs2106663441
gnomAD v3: 3-74578568-G-C
gnomAD v4: 3-74578568-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.74578568G>C , CM000665.2:g.74578568G>C GRCh38
NC_000003.11:g.74627719G>C , CM000665.1:g.74627719G>C GRCh37
NC_000003.10:g.74710409G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000263665.7:c.-81+35823C>G MANE Select ENSP00000263665.6:n.-81+35823C>G
XM_005264757.2:c.-81+35823C>G XP_005264814.1:n.-81+35823C>G
XM_005264758.2:c.-81+35823C>G XP_005264815.1:n.-81+35823C>G
XM_005264757.3:c.-81+35823C>G XP_005264814.1:n.-81+35823C>G
XM_017006507.1:c.-81+35180C>G XP_016861996.1:n.-81+35180C>G
NM_001393376.1:c.-81+35180C>G NP_001380305.1:n.-81+35180C>G
NM_020872.3:c.-81+35823C>G MANE Select NP_065923.1:n.-81+35823C>G
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