Canonical Allele Identifier: CA136637795
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1052709758
gnomAD v2: 6-24306453-A-G
gnomAD v3: 6-24306225-A-G
gnomAD v4: 6-24306225-A-G
MyVariant Identifiers: chr6:g.24306453A>G (hg19) chr6:g.24306225A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24306225A>G , CM000668.2:g.24306225A>G GRCh38
NC_000006.11:g.24306453A>G , CM000668.1:g.24306453A>G GRCh37
NC_000006.10:g.24414432A>G NCBI36
NG_012829.1:g.56828T>C
NG_012829.2:g.82068T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.349-4181T>C MANE Select ENSP00000367715.3:n.349-4181T>C
ENST00000378454.7:c.349-4181T>C ENSP00000367715.3:n.349-4181T>C
NM_001195610.1:c.349-4181T>C NP_001182539.1:n.349-4181T>C
NM_016356.4:c.349-4181T>C NP_057440.2:n.349-4181T>C
NM_016356.5:c.349-4181T>C MANE Select NP_057440.2:n.349-4181T>C
NM_001195610.2:c.349-4181T>C NP_001182539.1:n.349-4181T>C
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