Canonical Allele Identifier: CA1616417038
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs533586415

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24306241T>A , CM000668.2:g.24306241T>A GRCh38
NC_000006.11:g.24306469T>A , CM000668.1:g.24306469T>A GRCh37
NC_000006.10:g.24414448T>A NCBI36
NG_012829.1:g.56812A>T
NG_012829.2:g.82052A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.349-4197A>T MANE Select ENSP00000367715.3:n.349-4197A>T
ENST00000378454.7:c.349-4197A>T ENSP00000367715.3:n.349-4197A>T
NM_001195610.1:c.349-4197A>T NP_001182539.1:n.349-4197A>T
NM_016356.4:c.349-4197A>T NP_057440.2:n.349-4197A>T
NM_016356.5:c.349-4197A>T MANE Select NP_057440.2:n.349-4197A>T
NM_001195610.2:c.349-4197A>T NP_001182539.1:n.349-4197A>T