Canonical Allele Identifier: CA448963295
Gene: DCDC2 HGNC NCBI

Linked Data

gnomAD v4: 6-24178489-C-T
MyVariant Identifiers: chr6:g.24178717C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24178489C>T , CM000668.2:g.24178489C>T GRCh38
NC_000006.11:g.24178717C>T , CM000668.1:g.24178717C>T GRCh37
NC_000006.10:g.24286696C>T NCBI36
NG_012829.1:g.184564G>A
NG_012829.2:g.209804G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.1167G>A MANE Select ENSP00000367715.3:p.Glu389=
ENST00000378450.6:c.426G>A ENSP00000367711.3:p.Glu142=
ENST00000378454.7:c.1167G>A ENSP00000367715.3:p.Glu389=
NM_001195610.1:c.1167G>A NP_001182539.1:p.Glu389=
NM_016356.4:c.1167G>A NP_057440.2:p.Glu389=
NM_016356.5:c.1167G>A MANE Select NP_057440.2:p.Glu389=
NM_001195610.2:c.1167G>A NP_001182539.1:p.Glu389=
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