Canonical Allele Identifier: CA363281000
Gene: DCDC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24301768A>T , CM000668.2:g.24301768A>T GRCh38
NC_000006.11:g.24301996A>T , CM000668.1:g.24301996A>T GRCh37
NC_000006.10:g.24409975A>T NCBI36
NG_012829.1:g.61285T>A
NG_012829.2:g.86525T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.504T>A MANE Select ENSP00000367715.3:p.His168Gln
ENST00000378454.7:c.504T>A ENSP00000367715.3:p.His168Gln
NM_001195610.1:c.504T>A NP_001182539.1:p.His168Gln
NM_016356.4:c.504T>A NP_057440.2:p.His168Gln
NM_016356.5:c.504T>A MANE Select NP_057440.2:p.His168Gln
NM_001195610.2:c.504T>A NP_001182539.1:p.His168Gln