Canonical Allele Identifier: CA823284566
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1178916292
gnomAD v3: 6-24278678-TG-T
gnomAD v4: 6-24278678-TG-T
MyVariant Identifiers: chr6:g.24278907del (hg19) chr6:g.24278679del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24278679del , CM000668.2:g.24278679del GRCh38
NC_000006.11:g.24278907del , CM000668.1:g.24278907del GRCh37
NC_000006.10:g.24386886del NCBI36
NG_012829.1:g.84374del
NG_012829.2:g.109614del

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.760-468del MANE Select ENSP00000367715.3:n.760-468del
ENST00000378454.7:c.760-468del ENSP00000367715.3:n.760-468del
NM_001195610.1:c.760-468del NP_001182539.1:n.760-468del
NM_016356.4:c.760-468del NP_057440.2:n.760-468del
NM_016356.5:c.760-468del MANE Select NP_057440.2:n.760-468del
NM_001195610.2:c.760-468del NP_001182539.1:n.760-468del
Search 100 bp 5'
Search 100 bp 3'