Canonical Allele Identifier: CA2593679669
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs2113763203
gnomAD v3: 6-24207039-A-AT
gnomAD v4: 6-24207039-A-AT
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24207043dup , CM000668.2:g.24207043dup GRCh38
NC_000006.11:g.24207271dup , CM000668.1:g.24207271dup GRCh37
NC_000006.10:g.24315250dup NCBI36
NG_012829.1:g.156013dup
NG_012829.2:g.181253dup

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.923-1938dup MANE Select ENSP00000367715.3:n.923-1938dup
ENST00000378454.7:c.923-1938dup ENSP00000367715.3:n.923-1938dup
NM_001195610.1:c.923-1938dup NP_001182539.1:n.923-1938dup
NM_016356.4:c.923-1938dup NP_057440.2:n.923-1938dup
NM_016356.5:c.923-1938dup MANE Select NP_057440.2:n.923-1938dup
NM_001195610.2:c.923-1938dup NP_001182539.1:n.923-1938dup
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