Canonical Allele Identifier: CA3654725
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs776598401
gnomAD v2: 6-24301903-A-G
gnomAD v4: 6-24301675-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24301675A>G , CM000668.2:g.24301675A>G GRCh38
NC_000006.11:g.24301903A>G , CM000668.1:g.24301903A>G GRCh37
NC_000006.10:g.24409882A>G NCBI36
NG_012829.1:g.61378T>C
NG_012829.2:g.86618T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.557+40T>C MANE Select ENSP00000367715.3:n.557+40T>C
ENST00000378454.7:c.557+40T>C ENSP00000367715.3:n.557+40T>C
NM_001195610.1:c.557+40T>C NP_001182539.1:n.557+40T>C
NM_016356.4:c.557+40T>C NP_057440.2:n.557+40T>C
NM_016356.5:c.557+40T>C MANE Select NP_057440.2:n.557+40T>C
NM_001195610.2:c.557+40T>C NP_001182539.1:n.557+40T>C