Canonical Allele Identifier: CA566223199
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs377595278
gnomAD v2: 6-24291130-G-A
gnomAD v4: 6-24290902-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24290902G>A , CM000668.2:g.24290902G>A GRCh38
NC_000006.11:g.24291130G>A , CM000668.1:g.24291130G>A GRCh37
NC_000006.10:g.24399109G>A NCBI36
NG_012829.1:g.72151C>T
NG_012829.2:g.97391C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.704+30C>T MANE Select ENSP00000367715.3:n.704+30C>T
ENST00000378454.7:c.704+30C>T ENSP00000367715.3:n.704+30C>T
NM_001195610.1:c.704+30C>T NP_001182539.1:n.704+30C>T
NM_016356.4:c.704+30C>T NP_057440.2:n.704+30C>T
NM_016356.5:c.704+30C>T MANE Select NP_057440.2:n.704+30C>T
NM_001195610.2:c.704+30C>T NP_001182539.1:n.704+30C>T