Canonical Allele Identifier: CA1086944188
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1759467023
gnomAD v3: 6-24306022-C-G
gnomAD v4: 6-24306022-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24306022C>G , CM000668.2:g.24306022C>G GRCh38
NC_000006.11:g.24306250C>G , CM000668.1:g.24306250C>G GRCh37
NC_000006.10:g.24414229C>G NCBI36
NG_012829.1:g.57031G>C
NG_012829.2:g.82271G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.349-3978G>C MANE Select ENSP00000367715.3:n.349-3978G>C
ENST00000378454.7:c.349-3978G>C ENSP00000367715.3:n.349-3978G>C
NM_001195610.1:c.349-3978G>C NP_001182539.1:n.349-3978G>C
NM_016356.4:c.349-3978G>C NP_057440.2:n.349-3978G>C
NM_016356.5:c.349-3978G>C MANE Select NP_057440.2:n.349-3978G>C
NM_001195610.2:c.349-3978G>C NP_001182539.1:n.349-3978G>C
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