Canonical Allele Identifier: CA1086944177
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1759466550
gnomAD v3: 6-24305994-C-A
gnomAD v4: 6-24305994-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24305994C>A , CM000668.2:g.24305994C>A GRCh38
NC_000006.11:g.24306222C>A , CM000668.1:g.24306222C>A GRCh37
NC_000006.10:g.24414201C>A NCBI36
NG_012829.1:g.57059G>T
NG_012829.2:g.82299G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.349-3950G>T MANE Select ENSP00000367715.3:n.349-3950G>T
ENST00000378454.7:c.349-3950G>T ENSP00000367715.3:n.349-3950G>T
NM_001195610.1:c.349-3950G>T NP_001182539.1:n.349-3950G>T
NM_016356.4:c.349-3950G>T NP_057440.2:n.349-3950G>T
NM_016356.5:c.349-3950G>T MANE Select NP_057440.2:n.349-3950G>T
NM_001195610.2:c.349-3950G>T NP_001182539.1:n.349-3950G>T
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