Canonical Allele Identifier: CA823291019
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1161930314
gnomAD v3: 6-24290737-T-A
gnomAD v4: 6-24290737-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24290737T>A , CM000668.2:g.24290737T>A GRCh38
NC_000006.11:g.24290965T>A , CM000668.1:g.24290965T>A GRCh37
NC_000006.10:g.24398944T>A NCBI36
NG_012829.1:g.72316A>T
NG_012829.2:g.97556A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.704+195A>T MANE Select ENSP00000367715.3:n.704+195A>T
ENST00000378454.7:c.704+195A>T ENSP00000367715.3:n.704+195A>T
NM_001195610.1:c.704+195A>T NP_001182539.1:n.704+195A>T
NM_016356.4:c.704+195A>T NP_057440.2:n.704+195A>T
NM_016356.5:c.704+195A>T MANE Select NP_057440.2:n.704+195A>T
NM_001195610.2:c.704+195A>T NP_001182539.1:n.704+195A>T