Canonical Allele Identifier: CA1086937669
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1761722415
gnomAD v3: 6-24206656-A-C
gnomAD v4: 6-24206656-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24206656A>C , CM000668.2:g.24206656A>C GRCh38
NC_000006.11:g.24206884A>C , CM000668.1:g.24206884A>C GRCh37
NC_000006.10:g.24314863A>C NCBI36
NG_012829.1:g.156397T>G
NG_012829.2:g.181637T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.923-1554T>G MANE Select ENSP00000367715.3:n.923-1554T>G
ENST00000378454.7:c.923-1554T>G ENSP00000367715.3:n.923-1554T>G
NM_001195610.1:c.923-1554T>G NP_001182539.1:n.923-1554T>G
NM_016356.4:c.923-1554T>G NP_057440.2:n.923-1554T>G
NM_016356.5:c.923-1554T>G MANE Select NP_057440.2:n.923-1554T>G
NM_001195610.2:c.923-1554T>G NP_001182539.1:n.923-1554T>G
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