Canonical Allele Identifier: CA1086921730
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1760959584
gnomAD v3: 6-24177872-T-C
gnomAD v4: 6-24177872-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24177872T>C , CM000668.2:g.24177872T>C GRCh38
NC_000006.11:g.24178100T>C , CM000668.1:g.24178100T>C GRCh37
NC_000006.10:g.24286079T>C NCBI36
NG_012829.1:g.185181A>G
NG_012829.2:g.210421A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.1326+458A>G MANE Select ENSP00000367715.3:n.1326+458A>G
ENST00000378450.6:c.585+458A>G ENSP00000367711.3:n.585+458A>G
ENST00000378454.7:c.1326+458A>G ENSP00000367715.3:n.1326+458A>G
NM_001195610.1:c.1326+458A>G NP_001182539.1:n.1326+458A>G
NM_016356.4:c.1326+458A>G NP_057440.2:n.1326+458A>G
NM_016356.5:c.1326+458A>G MANE Select NP_057440.2:n.1326+458A>G
NM_001195610.2:c.1326+458A>G NP_001182539.1:n.1326+458A>G
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