Canonical Allele Identifier: CA448951161
Gene: DCDC2 HGNC NCBI

Linked Data

gnomAD v4: 6-24290934-A-G
MyVariant Identifiers: chr6:g.24291162A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24290934A>G , CM000668.2:g.24290934A>G GRCh38
NC_000006.11:g.24291162A>G , CM000668.1:g.24291162A>G GRCh37
NC_000006.10:g.24399141A>G NCBI36
NG_012829.1:g.72119T>C
NG_012829.2:g.97359T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.702T>C MANE Select ENSP00000367715.3:p.Phe234=
ENST00000378454.7:c.702T>C ENSP00000367715.3:p.Phe234=
NM_001195610.1:c.702T>C NP_001182539.1:p.Phe234=
NM_016356.4:c.702T>C NP_057440.2:p.Phe234=
NM_016356.5:c.702T>C MANE Select NP_057440.2:p.Phe234=
NM_001195610.2:c.702T>C NP_001182539.1:p.Phe234=