Canonical Allele Identifier: CA1616386110
Gene: DCDC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24206908C= , CM000668.2:g.24206908C= GRCh38
NC_000006.11:g.24207136C= , CM000668.1:g.24207136C= GRCh37
NC_000006.10:g.24315115C= NCBI36
NG_012829.1:g.156145G=
NG_012829.2:g.181385G=

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.923-1806G= MANE Select ENSP00000367715.3:n.923-1806G=
ENST00000378454.7:c.923-1806G= ENSP00000367715.3:n.923-1806G=
NM_001195610.1:c.923-1806G= NP_001182539.1:n.923-1806G=
NM_016356.4:c.923-1806G= NP_057440.2:n.923-1806G=
NM_016356.5:c.923-1806G= MANE Select NP_057440.2:n.923-1806G=
NM_001195610.2:c.923-1806G= NP_001182539.1:n.923-1806G=