Canonical Allele Identifier: CA1616386136
Gene: DCDC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24206967A= , CM000668.2:g.24206967A= GRCh38
NC_000006.11:g.24207195A= , CM000668.1:g.24207195A= GRCh37
NC_000006.10:g.24315174A= NCBI36
NG_012829.1:g.156086T=
NG_012829.2:g.181326T=

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.923-1865T= MANE Select ENSP00000367715.3:n.923-1865T=
ENST00000378454.7:c.923-1865T= ENSP00000367715.3:n.923-1865T=
NM_001195610.1:c.923-1865T= NP_001182539.1:n.923-1865T=
NM_016356.4:c.923-1865T= NP_057440.2:n.923-1865T=
NM_016356.5:c.923-1865T= MANE Select NP_057440.2:n.923-1865T=
NM_001195610.2:c.923-1865T= NP_001182539.1:n.923-1865T=