Canonical Allele Identifier: CA566214928
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1308808352
gnomAD v2: 6-24204821-C-T
gnomAD v3: 6-24204593-C-T
gnomAD v4: 6-24204593-C-T
MyVariant Identifiers: chr6:g.24204821C>T (hg19) chr6:g.24204593C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24204593C>T , CM000668.2:g.24204593C>T GRCh38
NC_000006.11:g.24204821C>T , CM000668.1:g.24204821C>T GRCh37
NC_000006.10:g.24312800C>T NCBI36
NG_012829.1:g.158460G>A
NG_012829.2:g.183700G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.1023+409G>A MANE Select ENSP00000367715.3:n.1023+409G>A
ENST00000378450.6:c.282+409G>A ENSP00000367711.3:n.282+409G>A
ENST00000378454.7:c.1023+409G>A ENSP00000367715.3:n.1023+409G>A
NM_001195610.1:c.1023+409G>A NP_001182539.1:n.1023+409G>A
NM_016356.4:c.1023+409G>A NP_057440.2:n.1023+409G>A
NM_016356.5:c.1023+409G>A MANE Select NP_057440.2:n.1023+409G>A
NM_001195610.2:c.1023+409G>A NP_001182539.1:n.1023+409G>A
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