Canonical Allele Identifier: CA1086937741
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1761725554
gnomAD v3: 6-24206833-T-C
gnomAD v4: 6-24206833-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24206833T>C , CM000668.2:g.24206833T>C GRCh38
NC_000006.11:g.24207061T>C , CM000668.1:g.24207061T>C GRCh37
NC_000006.10:g.24315040T>C NCBI36
NG_012829.1:g.156220A>G
NG_012829.2:g.181460A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.923-1731A>G MANE Select ENSP00000367715.3:n.923-1731A>G
ENST00000378454.7:c.923-1731A>G ENSP00000367715.3:n.923-1731A>G
NM_001195610.1:c.923-1731A>G NP_001182539.1:n.923-1731A>G
NM_016356.4:c.923-1731A>G NP_057440.2:n.923-1731A>G
NM_016356.5:c.923-1731A>G MANE Select NP_057440.2:n.923-1731A>G
NM_001195610.2:c.923-1731A>G NP_001182539.1:n.923-1731A>G