Canonical Allele Identifier: CA2677515219
Gene: DCDC2 HGNC NCBI

Linked Data

gnomAD v4: 6-24301589-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24301589A>T , CM000668.2:g.24301589A>T GRCh38
NC_000006.11:g.24301817A>T , CM000668.1:g.24301817A>T GRCh37
NC_000006.10:g.24409796A>T NCBI36
NG_012829.1:g.61464T>A
NG_012829.2:g.86704T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.557+126T>A MANE Select ENSP00000367715.3:n.557+126T>A
ENST00000378454.7:c.557+126T>A ENSP00000367715.3:n.557+126T>A
NM_001195610.1:c.557+126T>A NP_001182539.1:n.557+126T>A
NM_016356.4:c.557+126T>A NP_057440.2:n.557+126T>A
NM_016356.5:c.557+126T>A MANE Select NP_057440.2:n.557+126T>A
NM_001195610.2:c.557+126T>A NP_001182539.1:n.557+126T>A