Canonical Allele Identifier: CA136637776
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs904100050
gnomAD v2: 6-24306256-C-CA
gnomAD v3: 6-24306028-C-CA
gnomAD v4: 6-24306028-C-CA
MyVariant Identifiers: chr6:g.24306257_24306258insA (hg19) chr6:g.24306256_24306257insA (hg19) chr6:g.24306029_24306030insA (hg38) chr6:g.24306028_24306029insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24306038dup , CM000668.2:g.24306038dup GRCh38
NC_000006.11:g.24306266dup , CM000668.1:g.24306266dup GRCh37
NC_000006.10:g.24414245dup NCBI36
NG_012829.1:g.57024dup
NG_012829.2:g.82264dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.349-3985dup MANE Select ENSP00000367715.3:n.349-3985dup
ENST00000378454.7:c.349-3985dup ENSP00000367715.3:n.349-3985dup
NM_001195610.1:c.349-3985dup NP_001182539.1:n.349-3985dup
NM_016356.4:c.349-3985dup NP_057440.2:n.349-3985dup
NM_016356.5:c.349-3985dup MANE Select NP_057440.2:n.349-3985dup
NM_001195610.2:c.349-3985dup NP_001182539.1:n.349-3985dup
Search 100 bp 5'
Search 100 bp 3'