Canonical Allele Identifier: CA136622197
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs941074167
gnomAD v2: 6-24178442-C-A
gnomAD v3: 6-24178214-C-A
gnomAD v4: 6-24178214-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24178214C>A , CM000668.2:g.24178214C>A GRCh38
NC_000006.11:g.24178442C>A , CM000668.1:g.24178442C>A GRCh37
NC_000006.10:g.24286421C>A NCBI36
NG_012829.1:g.184839G>T
NG_012829.2:g.210079G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.1326+116G>T MANE Select ENSP00000367715.3:n.1326+116G>T
ENST00000378450.6:c.585+116G>T ENSP00000367711.3:n.585+116G>T
ENST00000378454.7:c.1326+116G>T ENSP00000367715.3:n.1326+116G>T
NM_001195610.1:c.1326+116G>T NP_001182539.1:n.1326+116G>T
NM_016356.4:c.1326+116G>T NP_057440.2:n.1326+116G>T
NM_016356.5:c.1326+116G>T MANE Select NP_057440.2:n.1326+116G>T
NM_001195610.2:c.1326+116G>T NP_001182539.1:n.1326+116G>T