Canonical Allele Identifier: CA2677493300
Gene: DCDC2 HGNC NCBI

Linked Data

gnomAD v4: 6-24278029-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24278029G>C , CM000668.2:g.24278029G>C GRCh38
NC_000006.11:g.24278257G>C , CM000668.1:g.24278257G>C GRCh37
NC_000006.10:g.24386236G>C NCBI36
NG_012829.1:g.85024C>G
NG_012829.2:g.110264C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.922+20C>G MANE Select ENSP00000367715.3:n.922+20C>G
ENST00000378454.7:c.922+20C>G ENSP00000367715.3:n.922+20C>G
NM_001195610.1:c.922+20C>G NP_001182539.1:n.922+20C>G
NM_016356.4:c.922+20C>G NP_057440.2:n.922+20C>G
NM_016356.5:c.922+20C>G MANE Select NP_057440.2:n.922+20C>G
NM_001195610.2:c.922+20C>G NP_001182539.1:n.922+20C>G
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