Canonical Allele Identifier: CA2677515082
Gene: DCDC2 HGNC NCBI

Linked Data

gnomAD v4: 6-24290795-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24290795G>A , CM000668.2:g.24290795G>A GRCh38
NC_000006.11:g.24291023G>A , CM000668.1:g.24291023G>A GRCh37
NC_000006.10:g.24399002G>A NCBI36
NG_012829.1:g.72258C>T
NG_012829.2:g.97498C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.704+137C>T MANE Select ENSP00000367715.3:n.704+137C>T
ENST00000378454.7:c.704+137C>T ENSP00000367715.3:n.704+137C>T
NM_001195610.1:c.704+137C>T NP_001182539.1:n.704+137C>T
NM_016356.4:c.704+137C>T NP_057440.2:n.704+137C>T
NM_016356.5:c.704+137C>T MANE Select NP_057440.2:n.704+137C>T
NM_001195610.2:c.704+137C>T NP_001182539.1:n.704+137C>T