Canonical Allele Identifier: CA2677514144
Gene: DCDC2 HGNC NCBI

Linked Data

gnomAD v4: 6-24174695-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24174695T>C , CM000668.2:g.24174695T>C GRCh38
NC_000006.11:g.24174923T>C , CM000668.1:g.24174923T>C GRCh37
NC_000006.10:g.24282902T>C NCBI36
NG_012829.1:g.188358A>G
NG_012829.2:g.213598A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.*35A>G MANE Select ENSP00000367715.3:n.*35A>G
ENST00000378450.6:c.*35A>G ENSP00000367711.3:n.*35A>G
ENST00000378454.7:c.*35A>G ENSP00000367715.3:n.*35A>G
NM_001195610.1:c.*35A>G NP_001182539.1:n.*35A>G
NM_016356.4:c.*35A>G NP_057440.2:n.*35A>G
NM_016356.5:c.*35A>G MANE Select NP_057440.2:n.*35A>G
NM_001195610.2:c.*35A>G NP_001182539.1:n.*35A>G
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