Canonical Allele Identifier: CA2677493212
Gene: DCDC2 HGNC NCBI

Linked Data

gnomAD v4: 6-24277903-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24277903C>A , CM000668.2:g.24277903C>A GRCh38
NC_000006.11:g.24278131C>A , CM000668.1:g.24278131C>A GRCh37
NC_000006.10:g.24386110C>A NCBI36
NG_012829.1:g.85150G>T
NG_012829.2:g.110390G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.922+146G>T MANE Select ENSP00000367715.3:n.922+146G>T
ENST00000378454.7:c.922+146G>T ENSP00000367715.3:n.922+146G>T
NM_001195610.1:c.922+146G>T NP_001182539.1:n.922+146G>T
NM_016356.4:c.922+146G>T NP_057440.2:n.922+146G>T
NM_016356.5:c.922+146G>T MANE Select NP_057440.2:n.922+146G>T
NM_001195610.2:c.922+146G>T NP_001182539.1:n.922+146G>T