Canonical Allele Identifier: CA566291275
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1332619367
gnomAD v2: 6-24278263-A-T
gnomAD v4: 6-24278035-A-T
MyVariant Identifiers: chr6:g.24278263A>T (hg19) chr6:g.24278035A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24278035A>T , CM000668.2:g.24278035A>T GRCh38
NC_000006.11:g.24278263A>T , CM000668.1:g.24278263A>T GRCh37
NC_000006.10:g.24386242A>T NCBI36
NG_012829.1:g.85018T>A
NG_012829.2:g.110258T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.922+14T>A MANE Select ENSP00000367715.3:n.922+14T>A
ENST00000378454.7:c.922+14T>A ENSP00000367715.3:n.922+14T>A
NM_001195610.1:c.922+14T>A NP_001182539.1:n.922+14T>A
NM_016356.4:c.922+14T>A NP_057440.2:n.922+14T>A
NM_016356.5:c.922+14T>A MANE Select NP_057440.2:n.922+14T>A
NM_001195610.2:c.922+14T>A NP_001182539.1:n.922+14T>A
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