Canonical Allele Identifier: CA363277448
Gene: DCDC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.24205260T>A (hg19) chr6:g.24205032T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24205032T>A , CM000668.2:g.24205032T>A GRCh38
NC_000006.11:g.24205260T>A , CM000668.1:g.24205260T>A GRCh37
NC_000006.10:g.24313239T>A NCBI36
NG_012829.1:g.158021A>T
NG_012829.2:g.183261A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.993A>T MANE Select ENSP00000367715.3:p.Glu331Asp
ENST00000378450.6:c.252A>T ENSP00000367711.3:p.Glu84Asp
ENST00000378454.7:c.993A>T ENSP00000367715.3:p.Glu331Asp
NM_001195610.1:c.993A>T NP_001182539.1:p.Glu331Asp
NM_016356.4:c.993A>T NP_057440.2:p.Glu331Asp
NM_016356.5:c.993A>T MANE Select NP_057440.2:p.Glu331Asp
NM_001195610.2:c.993A>T NP_001182539.1:p.Glu331Asp
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