Canonical Allele Identifier: CA136637800
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs200698844
gnomAD v2: 6-24306489-TC-T
gnomAD v3: 6-24306261-TC-T
gnomAD v4: 6-24306261-TC-T
MyVariant Identifiers: chr6:g.24306490del (hg19) chr6:g.24306262del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24306262del , CM000668.2:g.24306262del GRCh38
NC_000006.11:g.24306490del , CM000668.1:g.24306490del GRCh37
NC_000006.10:g.24414469del NCBI36
NG_012829.1:g.56791del
NG_012829.2:g.82031del

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.349-4218del MANE Select ENSP00000367715.3:n.349-4218del
ENST00000378454.7:c.349-4218del ENSP00000367715.3:n.349-4218del
NM_001195610.1:c.349-4218del NP_001182539.1:n.349-4218del
NM_016356.4:c.349-4218del NP_057440.2:n.349-4218del
NM_016356.5:c.349-4218del MANE Select NP_057440.2:n.349-4218del
NM_001195610.2:c.349-4218del NP_001182539.1:n.349-4218del
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