Canonical Allele Identifier: CA566291326
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1296554840
gnomAD v2: 6-24302178-TA-T
gnomAD v4: 6-24301950-TA-T
MyVariant Identifiers: chr6:g.24302179del (hg19) chr6:g.24301951del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24301953del , CM000668.2:g.24301953del GRCh38
NC_000006.11:g.24302181del , CM000668.1:g.24302181del GRCh37
NC_000006.10:g.24410160del NCBI36
NG_012829.1:g.61102del
NG_012829.2:g.86342del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.425+17del MANE Select ENSP00000367715.3:n.425+17del
ENST00000378454.7:c.425+17del ENSP00000367715.3:n.425+17del
NM_001195610.1:c.425+17del NP_001182539.1:n.425+17del
NM_016356.4:c.425+17del NP_057440.2:n.425+17del
NM_016356.5:c.425+17del MANE Select NP_057440.2:n.425+17del
NM_001195610.2:c.425+17del NP_001182539.1:n.425+17del
Search 100 bp 5'
Search 100 bp 3'