Canonical Allele Identifier: CA2677493236
Gene: DCDC2 HGNC NCBI

Linked Data

gnomAD v4: 6-24277950-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24277950A>C , CM000668.2:g.24277950A>C GRCh38
NC_000006.11:g.24278178A>C , CM000668.1:g.24278178A>C GRCh37
NC_000006.10:g.24386157A>C NCBI36
NG_012829.1:g.85103T>G
NG_012829.2:g.110343T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.922+99T>G MANE Select ENSP00000367715.3:n.922+99T>G
ENST00000378454.7:c.922+99T>G ENSP00000367715.3:n.922+99T>G
NM_001195610.1:c.922+99T>G NP_001182539.1:n.922+99T>G
NM_016356.4:c.922+99T>G NP_057440.2:n.922+99T>G
NM_016356.5:c.922+99T>G MANE Select NP_057440.2:n.922+99T>G
NM_001195610.2:c.922+99T>G NP_001182539.1:n.922+99T>G