Canonical Allele Identifier: CA1616325114
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1419228

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24178078G>C , CM000668.2:g.24178078G>C GRCh38
NC_000006.11:g.24178306G>C , CM000668.1:g.24178306G>C GRCh37
NC_000006.10:g.24286285G>C NCBI36
NG_012829.1:g.184975C>G
NG_012829.2:g.210215C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.1326+252C>G MANE Select ENSP00000367715.3:n.1326+252C>G
ENST00000378450.6:c.585+252C>G ENSP00000367711.3:n.585+252C>G
ENST00000378454.7:c.1326+252C>G ENSP00000367715.3:n.1326+252C>G
NM_001195610.1:c.1326+252C>G NP_001182539.1:n.1326+252C>G
NM_016356.4:c.1326+252C>G NP_057440.2:n.1326+252C>G
NM_016356.5:c.1326+252C>G MANE Select NP_057440.2:n.1326+252C>G
NM_001195610.2:c.1326+252C>G NP_001182539.1:n.1326+252C>G