Canonical Allele Identifier: CA136642201
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs955305073
gnomAD v2: 6-24348093-C-T
gnomAD v3: 6-24347865-C-T
gnomAD v4: 6-24347865-C-T
MyVariant Identifiers: chr6:g.24348093C>T (hg19) chr6:g.24347865C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24347865C>T , CM000668.2:g.24347865C>T GRCh38
NC_000006.11:g.24348093C>T , CM000668.1:g.24348093C>T GRCh37
NC_000006.10:g.24456072C>T NCBI36
NG_012829.1:g.15188G>A
NG_012829.2:g.40428G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.348+5704G>A MANE Select ENSP00000367715.3:n.348+5704G>A
ENST00000378454.7:c.348+5704G>A ENSP00000367715.3:n.348+5704G>A
NM_001195610.1:c.348+5704G>A NP_001182539.1:n.348+5704G>A
NM_016356.4:c.348+5704G>A NP_057440.2:n.348+5704G>A
NM_016356.5:c.348+5704G>A MANE Select NP_057440.2:n.348+5704G>A
NM_001195610.2:c.348+5704G>A NP_001182539.1:n.348+5704G>A
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