Canonical Allele Identifier: CA1616386113
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1761726807

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24206909C>T , CM000668.2:g.24206909C>T GRCh38
NC_000006.11:g.24207137C>T , CM000668.1:g.24207137C>T GRCh37
NC_000006.10:g.24315116C>T NCBI36
NG_012829.1:g.156144G>A
NG_012829.2:g.181384G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.923-1807G>A MANE Select ENSP00000367715.3:n.923-1807G>A
ENST00000378454.7:c.923-1807G>A ENSP00000367715.3:n.923-1807G>A
NM_001195610.1:c.923-1807G>A NP_001182539.1:n.923-1807G>A
NM_016356.4:c.923-1807G>A NP_057440.2:n.923-1807G>A
NM_016356.5:c.923-1807G>A MANE Select NP_057440.2:n.923-1807G>A
NM_001195610.2:c.923-1807G>A NP_001182539.1:n.923-1807G>A