Canonical Allele Identifier: CA363280257
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1763729674
gnomAD v3: 6-24290958-G-T
gnomAD v4: 6-24290958-G-T
MyVariant Identifiers: chr6:g.24291186G>T (hg19) chr6:g.24290958G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24290958G>T , CM000668.2:g.24290958G>T GRCh38
NC_000006.11:g.24291186G>T , CM000668.1:g.24291186G>T GRCh37
NC_000006.10:g.24399165G>T NCBI36
NG_012829.1:g.72095C>A
NG_012829.2:g.97335C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.678C>A MANE Select ENSP00000367715.3:p.Asp226Glu
ENST00000378454.7:c.678C>A ENSP00000367715.3:p.Asp226Glu
NM_001195610.1:c.678C>A NP_001182539.1:p.Asp226Glu
NM_016356.4:c.678C>A NP_057440.2:p.Asp226Glu
NM_016356.5:c.678C>A MANE Select NP_057440.2:p.Asp226Glu
NM_001195610.2:c.678C>A NP_001182539.1:p.Asp226Glu
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