Canonical Allele Identifier: CA136621781
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs11557307
gnomAD v2: 6-24174924-C-T
gnomAD v4: 6-24174696-C-T
MyVariant Identifiers: chr6:g.24174924C>T (hg19) chr6:g.24174696C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24174696C>T , CM000668.2:g.24174696C>T GRCh38
NC_000006.11:g.24174924C>T , CM000668.1:g.24174924C>T GRCh37
NC_000006.10:g.24282903C>T NCBI36
NG_012829.1:g.188357G>A
NG_012829.2:g.213597G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.*34G>A MANE Select ENSP00000367715.3:n.*34G>A
ENST00000378450.6:c.*34G>A ENSP00000367711.3:n.*34G>A
ENST00000378454.7:c.*34G>A ENSP00000367715.3:n.*34G>A
NM_001195610.1:c.*34G>A NP_001182539.1:n.*34G>A
NM_016356.4:c.*34G>A NP_057440.2:n.*34G>A
NM_016356.5:c.*34G>A MANE Select NP_057440.2:n.*34G>A
NM_001195610.2:c.*34G>A NP_001182539.1:n.*34G>A
Search 100 bp 5'
Search 100 bp 3'