Canonical Allele Identifier: CA448951432
Gene: DCDC2 HGNC NCBI

Linked Data

gnomAD v4: 6-24302021-C-T
MyVariant Identifiers: chr6:g.24302249C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24302021C>T , CM000668.2:g.24302021C>T GRCh38
NC_000006.11:g.24302249C>T , CM000668.1:g.24302249C>T GRCh37
NC_000006.10:g.24410228C>T NCBI36
NG_012829.1:g.61032G>A
NG_012829.2:g.86272G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.372G>A MANE Select ENSP00000367715.3:p.Arg124=
ENST00000378454.7:c.372G>A ENSP00000367715.3:p.Arg124=
NM_001195610.1:c.372G>A NP_001182539.1:p.Arg124=
NM_016356.4:c.372G>A NP_057440.2:p.Arg124=
NM_016356.5:c.372G>A MANE Select NP_057440.2:p.Arg124=
NM_001195610.2:c.372G>A NP_001182539.1:p.Arg124=
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