Canonical Allele Identifier: CA1616386082
Gene: DCDC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24206855C= , CM000668.2:g.24206855C= GRCh38
NC_000006.11:g.24207083C= , CM000668.1:g.24207083C= GRCh37
NC_000006.10:g.24315062C= NCBI36
NG_012829.1:g.156198G=
NG_012829.2:g.181438G=

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.923-1753G= MANE Select ENSP00000367715.3:n.923-1753G=
ENST00000378454.7:c.923-1753G= ENSP00000367715.3:n.923-1753G=
NM_001195610.1:c.923-1753G= NP_001182539.1:n.923-1753G=
NM_016356.4:c.923-1753G= NP_057440.2:n.923-1753G=
NM_016356.5:c.923-1753G= MANE Select NP_057440.2:n.923-1753G=
NM_001195610.2:c.923-1753G= NP_001182539.1:n.923-1753G=