Canonical Allele Identifier: CA566215095
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1447526807
gnomAD v2: 6-24206864-GA-G
gnomAD v3: 6-24206636-GA-G
gnomAD v4: 6-24206636-GA-G
MyVariant Identifiers: chr6:g.24206865del (hg19) chr6:g.24206637del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24206639del , CM000668.2:g.24206639del GRCh38
NC_000006.11:g.24206867del , CM000668.1:g.24206867del GRCh37
NC_000006.10:g.24314846del NCBI36
NG_012829.1:g.156416del
NG_012829.2:g.181656del

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.923-1535del MANE Select ENSP00000367715.3:n.923-1535del
ENST00000378454.7:c.923-1535del ENSP00000367715.3:n.923-1535del
NM_001195610.1:c.923-1535del NP_001182539.1:n.923-1535del
NM_016356.4:c.923-1535del NP_057440.2:n.923-1535del
NM_016356.5:c.923-1535del MANE Select NP_057440.2:n.923-1535del
NM_001195610.2:c.923-1535del NP_001182539.1:n.923-1535del
Search 100 bp 5'
Search 100 bp 3'