Canonical Allele Identifier: CA448951164
Gene: DCDC2 HGNC NCBI

Linked Data

gnomAD v4: 6-24290937-A-T
MyVariant Identifiers: chr6:g.24291165A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24290937A>T , CM000668.2:g.24290937A>T GRCh38
NC_000006.11:g.24291165A>T , CM000668.1:g.24291165A>T GRCh37
NC_000006.10:g.24399144A>T NCBI36
NG_012829.1:g.72116T>A
NG_012829.2:g.97356T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.699T>A MANE Select ENSP00000367715.3:p.Pro233=
ENST00000378454.7:c.699T>A ENSP00000367715.3:p.Pro233=
NM_001195610.1:c.699T>A NP_001182539.1:p.Pro233=
NM_016356.4:c.699T>A NP_057440.2:p.Pro233=
NM_016356.5:c.699T>A MANE Select NP_057440.2:p.Pro233=
NM_001195610.2:c.699T>A NP_001182539.1:p.Pro233=