Canonical Allele Identifier: CA136634489
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1051533578
gnomAD v3: 6-24278549-C-T
gnomAD v4: 6-24278549-C-T
MyVariant Identifiers: chr6:g.24278777C>T (hg19) chr6:g.24278549C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24278549C>T , CM000668.2:g.24278549C>T GRCh38
NC_000006.11:g.24278777C>T , CM000668.1:g.24278777C>T GRCh37
NC_000006.10:g.24386756C>T NCBI36
NG_012829.1:g.84504G>A
NG_012829.2:g.109744G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.760-338G>A MANE Select ENSP00000367715.3:n.760-338G>A
ENST00000378454.7:c.760-338G>A ENSP00000367715.3:n.760-338G>A
NM_001195610.1:c.760-338G>A NP_001182539.1:n.760-338G>A
NM_016356.4:c.760-338G>A NP_057440.2:n.760-338G>A
NM_016356.5:c.760-338G>A MANE Select NP_057440.2:n.760-338G>A
NM_001195610.2:c.760-338G>A NP_001182539.1:n.760-338G>A
Search 100 bp 5'
Search 100 bp 3'