Canonical Allele Identifier: CA12317751
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs6922023

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24347889G>A , CM000668.2:g.24347889G>A GRCh38
NC_000006.11:g.24348117G>A , CM000668.1:g.24348117G>A GRCh37
NC_000006.10:g.24456096G>A NCBI36
NG_012829.1:g.15164C>T
NG_012829.2:g.40404C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.348+5680C>T MANE Select ENSP00000367715.3:n.348+5680C>T
ENST00000378454.7:c.348+5680C>T ENSP00000367715.3:n.348+5680C>T
NM_001195610.1:c.348+5680C>T NP_001182539.1:n.348+5680C>T
NM_016356.4:c.348+5680C>T NP_057440.2:n.348+5680C>T
NM_016356.5:c.348+5680C>T MANE Select NP_057440.2:n.348+5680C>T
NM_001195610.2:c.348+5680C>T NP_001182539.1:n.348+5680C>T