Canonical Allele Identifier: CA363279978
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1369820281
gnomAD v2: 6-24178657-A-T
gnomAD v3: 6-24178429-A-T
gnomAD v4: 6-24178429-A-T
MyVariant Identifiers: chr6:g.24178657A>T (hg19) chr6:g.24178429A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24178429A>T , CM000668.2:g.24178429A>T GRCh38
NC_000006.11:g.24178657A>T , CM000668.1:g.24178657A>T GRCh37
NC_000006.10:g.24286636A>T NCBI36
NG_012829.1:g.184624T>A
NG_012829.2:g.209864T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.1227T>A MANE Select ENSP00000367715.3:p.Asp409Glu
ENST00000378450.6:c.486T>A ENSP00000367711.3:p.Asp162Glu
ENST00000378454.7:c.1227T>A ENSP00000367715.3:p.Asp409Glu
NM_001195610.1:c.1227T>A NP_001182539.1:p.Asp409Glu
NM_016356.4:c.1227T>A NP_057440.2:p.Asp409Glu
NM_016356.5:c.1227T>A MANE Select NP_057440.2:p.Asp409Glu
NM_001195610.2:c.1227T>A NP_001182539.1:p.Asp409Glu
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