Canonical Allele Identifier: CA363280884
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs763299947

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24301714C>G , CM000668.2:g.24301714C>G GRCh38
NC_000006.11:g.24301942C>G , CM000668.1:g.24301942C>G GRCh37
NC_000006.10:g.24409921C>G NCBI36
NG_012829.1:g.61339G>C
NG_012829.2:g.86579G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.557+1G>C MANE Select ENSP00000367715.3:n.557+1G>C
ENST00000378454.7:c.557+1G>C ENSP00000367715.3:n.557+1G>C
NM_001195610.1:c.557+1G>C NP_001182539.1:n.557+1G>C
NM_016356.4:c.557+1G>C NP_057440.2:n.557+1G>C
NM_016356.5:c.557+1G>C MANE Select NP_057440.2:n.557+1G>C
NM_001195610.2:c.557+1G>C NP_001182539.1:n.557+1G>C