Canonical Allele Identifier: CA1616406494
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1760300153
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24348053G>A , CM000668.2:g.24348053G>A GRCh38
NC_000006.11:g.24348281G>A , CM000668.1:g.24348281G>A GRCh37
NC_000006.10:g.24456260G>A NCBI36
NG_012829.1:g.15000C>T
NG_012829.2:g.40240C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.348+5516C>T MANE Select ENSP00000367715.3:n.348+5516C>T
ENST00000378454.7:c.348+5516C>T ENSP00000367715.3:n.348+5516C>T
NM_001195610.1:c.348+5516C>T NP_001182539.1:n.348+5516C>T
NM_016356.4:c.348+5516C>T NP_057440.2:n.348+5516C>T
NM_016356.5:c.348+5516C>T MANE Select NP_057440.2:n.348+5516C>T
NM_001195610.2:c.348+5516C>T NP_001182539.1:n.348+5516C>T
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