Canonical Allele Identifier: CA136633925
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs565745830

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24273479G>A , CM000668.2:g.24273479G>A GRCh38
NC_000006.11:g.24273707G>A , CM000668.1:g.24273707G>A GRCh37
NC_000006.10:g.24381686G>A NCBI36
NG_012829.1:g.89574C>T
NG_012829.2:g.114814C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.922+4570C>T MANE Select ENSP00000367715.3:n.922+4570C>T
ENST00000378454.7:c.922+4570C>T ENSP00000367715.3:n.922+4570C>T
NM_001195610.1:c.922+4570C>T NP_001182539.1:n.922+4570C>T
NM_016356.4:c.922+4570C>T NP_057440.2:n.922+4570C>T
NM_016356.5:c.922+4570C>T MANE Select NP_057440.2:n.922+4570C>T
NM_001195610.2:c.922+4570C>T NP_001182539.1:n.922+4570C>T