Canonical Allele Identifier: CA1616386109
Gene: DCDC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24206907A= , CM000668.2:g.24206907A= GRCh38
NC_000006.11:g.24207135A= , CM000668.1:g.24207135A= GRCh37
NC_000006.10:g.24315114A= NCBI36
NG_012829.1:g.156146T=
NG_012829.2:g.181386T=

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.923-1805T= MANE Select ENSP00000367715.3:n.923-1805T=
ENST00000378454.7:c.923-1805T= ENSP00000367715.3:n.923-1805T=
NM_001195610.1:c.923-1805T= NP_001182539.1:n.923-1805T=
NM_016356.4:c.923-1805T= NP_057440.2:n.923-1805T=
NM_016356.5:c.923-1805T= MANE Select NP_057440.2:n.923-1805T=
NM_001195610.2:c.923-1805T= NP_001182539.1:n.923-1805T=