Canonical Allele Identifier: CA1616324846
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1760959652

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24177884G>C , CM000668.2:g.24177884G>C GRCh38
NC_000006.11:g.24178112G>C , CM000668.1:g.24178112G>C GRCh37
NC_000006.10:g.24286091G>C NCBI36
NG_012829.1:g.185169C>G
NG_012829.2:g.210409C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.1326+446C>G MANE Select ENSP00000367715.3:n.1326+446C>G
ENST00000378450.6:c.585+446C>G ENSP00000367711.3:n.585+446C>G
ENST00000378454.7:c.1326+446C>G ENSP00000367715.3:n.1326+446C>G
NM_001195610.1:c.1326+446C>G NP_001182539.1:n.1326+446C>G
NM_016356.4:c.1326+446C>G NP_057440.2:n.1326+446C>G
NM_016356.5:c.1326+446C>G MANE Select NP_057440.2:n.1326+446C>G
NM_001195610.2:c.1326+446C>G NP_001182539.1:n.1326+446C>G