Canonical Allele Identifier: CA136642177
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs989563421
gnomAD v3: 6-24347665-G-A
gnomAD v4: 6-24347665-G-A
MyVariant Identifiers: chr6:g.24347893G>A (hg19) chr6:g.24347665G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24347665G>A , CM000668.2:g.24347665G>A GRCh38
NC_000006.11:g.24347893G>A , CM000668.1:g.24347893G>A GRCh37
NC_000006.10:g.24455872G>A NCBI36
NG_012829.1:g.15388C>T
NG_012829.2:g.40628C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.348+5904C>T MANE Select ENSP00000367715.3:n.348+5904C>T
ENST00000378454.7:c.348+5904C>T ENSP00000367715.3:n.348+5904C>T
NM_001195610.1:c.348+5904C>T NP_001182539.1:n.348+5904C>T
NM_016356.4:c.348+5904C>T NP_057440.2:n.348+5904C>T
NM_016356.5:c.348+5904C>T MANE Select NP_057440.2:n.348+5904C>T
NM_001195610.2:c.348+5904C>T NP_001182539.1:n.348+5904C>T
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