Canonical Allele Identifier: CA566291238
Gene: DCDC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24178324A>C , CM000668.2:g.24178324A>C GRCh38
NC_000006.11:g.24178552A>C , CM000668.1:g.24178552A>C GRCh37
NC_000006.10:g.24286531A>C NCBI36
NG_012829.1:g.184729T>G
NG_012829.2:g.209969T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.1326+6T>G MANE Select ENSP00000367715.3:n.1326+6T>G
ENST00000378450.6:c.585+6T>G ENSP00000367711.3:n.585+6T>G
ENST00000378454.7:c.1326+6T>G ENSP00000367715.3:n.1326+6T>G
NM_001195610.1:c.1326+6T>G NP_001182539.1:n.1326+6T>G
NM_016356.4:c.1326+6T>G NP_057440.2:n.1326+6T>G
NM_016356.5:c.1326+6T>G MANE Select NP_057440.2:n.1326+6T>G
NM_001195610.2:c.1326+6T>G NP_001182539.1:n.1326+6T>G