Canonical Allele Identifier: CA1616429001
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1763411700
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24278696C>G , CM000668.2:g.24278696C>G GRCh38
NC_000006.11:g.24278924C>G , CM000668.1:g.24278924C>G GRCh37
NC_000006.10:g.24386903C>G NCBI36
NG_012829.1:g.84357G>C
NG_012829.2:g.109597G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.760-485G>C MANE Select ENSP00000367715.3:n.760-485G>C
ENST00000378454.7:c.760-485G>C ENSP00000367715.3:n.760-485G>C
NM_001195610.1:c.760-485G>C NP_001182539.1:n.760-485G>C
NM_016356.4:c.760-485G>C NP_057440.2:n.760-485G>C
NM_016356.5:c.760-485G>C MANE Select NP_057440.2:n.760-485G>C
NM_001195610.2:c.760-485G>C NP_001182539.1:n.760-485G>C
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