Canonical Allele Identifier: CA3654699
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs748783386

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24290976G>A , CM000668.2:g.24290976G>A GRCh38
NC_000006.11:g.24291204G>A , CM000668.1:g.24291204G>A GRCh37
NC_000006.10:g.24399183G>A NCBI36
NG_012829.1:g.72077C>T
NG_012829.2:g.97317C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.660C>T MANE Select ENSP00000367715.3:p.Tyr220=
ENST00000378454.7:c.660C>T ENSP00000367715.3:p.Tyr220=
NM_001195610.1:c.660C>T NP_001182539.1:p.Tyr220=
NM_016356.4:c.660C>T NP_057440.2:p.Tyr220=
NM_016356.5:c.660C>T MANE Select NP_057440.2:p.Tyr220=
NM_001195610.2:c.660C>T NP_001182539.1:p.Tyr220=