Canonical Allele Identifier: CA1086928556
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1760292734
gnomAD v3: 6-24347714-T-G
gnomAD v4: 6-24347714-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24347714T>G , CM000668.2:g.24347714T>G GRCh38
NC_000006.11:g.24347942T>G , CM000668.1:g.24347942T>G GRCh37
NC_000006.10:g.24455921T>G NCBI36
NG_012829.1:g.15339A>C
NG_012829.2:g.40579A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.348+5855A>C MANE Select ENSP00000367715.3:n.348+5855A>C
ENST00000378454.7:c.348+5855A>C ENSP00000367715.3:n.348+5855A>C
NM_001195610.1:c.348+5855A>C NP_001182539.1:n.348+5855A>C
NM_016356.4:c.348+5855A>C NP_057440.2:n.348+5855A>C
NM_016356.5:c.348+5855A>C MANE Select NP_057440.2:n.348+5855A>C
NM_001195610.2:c.348+5855A>C NP_001182539.1:n.348+5855A>C