Canonical Allele Identifier: CA363279773
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs375119774
gnomAD v2: 6-24178601-T-C
gnomAD v4: 6-24178373-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24178373T>C , CM000668.2:g.24178373T>C GRCh38
NC_000006.11:g.24178601T>C , CM000668.1:g.24178601T>C GRCh37
NC_000006.10:g.24286580T>C NCBI36
NG_012829.1:g.184680A>G
NG_012829.2:g.209920A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.1283A>G MANE Select ENSP00000367715.3:p.Asp428Gly
ENST00000378450.6:c.542A>G ENSP00000367711.3:p.Asp181Gly
ENST00000378454.7:c.1283A>G ENSP00000367715.3:p.Asp428Gly
NM_001195610.1:c.1283A>G NP_001182539.1:p.Asp428Gly
NM_016356.4:c.1283A>G NP_057440.2:p.Asp428Gly
NM_016356.5:c.1283A>G MANE Select NP_057440.2:p.Asp428Gly
NM_001195610.2:c.1283A>G NP_001182539.1:p.Asp428Gly