Canonical Allele Identifier: CA1616446762
Gene: DCDC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24290951T= , CM000668.2:g.24290951T= GRCh38
NC_000006.11:g.24291179T= , CM000668.1:g.24291179T= GRCh37
NC_000006.10:g.24399158T= NCBI36
NG_012829.1:g.72102A=
NG_012829.2:g.97342A=

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.685A= MANE Select ENSP00000367715.3:p.Thr229=
ENST00000378454.7:c.685A= ENSP00000367715.3:p.Thr229=
NM_001195610.1:c.685A= NP_001182539.1:p.Thr229=
NM_016356.4:c.685A= NP_057440.2:p.Thr229=
NM_016356.5:c.685A= MANE Select NP_057440.2:p.Thr229=
NM_001195610.2:c.685A= NP_001182539.1:p.Thr229=