Canonical Allele Identifier: CA3654499
Gene: DCDC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 707242
ClinVar RCV Id: RCV002064905
dbSNP Id: rs767129413
gnomAD v2: 6-24178720-G-A
gnomAD v3: 6-24178492-G-A
gnomAD v4: 6-24178492-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24178492G>A , CM000668.2:g.24178492G>A GRCh38
NC_000006.11:g.24178720G>A , CM000668.1:g.24178720G>A GRCh37
NC_000006.10:g.24286699G>A NCBI36
NG_012829.1:g.184561C>T
NG_012829.2:g.209801C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.1164C>T MANE Select ENSP00000367715.3:p.Val388=
ENST00000378450.6:c.423C>T ENSP00000367711.3:p.Val141=
ENST00000378454.7:c.1164C>T ENSP00000367715.3:p.Val388=
NM_001195610.1:c.1164C>T NP_001182539.1:p.Val388=
NM_016356.4:c.1164C>T NP_057440.2:p.Val388=
NM_016356.5:c.1164C>T MANE Select NP_057440.2:p.Val388=
NM_001195610.2:c.1164C>T NP_001182539.1:p.Val388=