Canonical Allele Identifier: CA566220582
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1260290896
gnomAD v2: 6-24174931-T-C
gnomAD v3: 6-24174703-T-C
gnomAD v4: 6-24174703-T-C
MyVariant Identifiers: chr6:g.24174931T>C (hg19) chr6:g.24174703T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24174703T>C , CM000668.2:g.24174703T>C GRCh38
NC_000006.11:g.24174931T>C , CM000668.1:g.24174931T>C GRCh37
NC_000006.10:g.24282910T>C NCBI36
NG_012829.1:g.188350A>G
NG_012829.2:g.213590A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.*27A>G MANE Select ENSP00000367715.3:n.*27A>G
ENST00000378450.6:c.*27A>G ENSP00000367711.3:n.*27A>G
ENST00000378454.7:c.*27A>G ENSP00000367715.3:n.*27A>G
NM_001195610.1:c.*27A>G NP_001182539.1:n.*27A>G
NM_016356.4:c.*27A>G NP_057440.2:n.*27A>G
NM_016356.5:c.*27A>G MANE Select NP_057440.2:n.*27A>G
NM_001195610.2:c.*27A>G NP_001182539.1:n.*27A>G
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