Canonical Allele Identifier: CA363277960
Gene: DCDC2 HGNC NCBI

Linked Data

COSMIC: COSM4924568
MyVariant Identifiers: chr6:g.24278324T>A (hg19) chr6:g.24278096T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24278096T>A , CM000668.2:g.24278096T>A GRCh38
NC_000006.11:g.24278324T>A , CM000668.1:g.24278324T>A GRCh37
NC_000006.10:g.24386303T>A NCBI36
NG_012829.1:g.84957A>T
NG_012829.2:g.110197A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.875A>T MANE Select ENSP00000367715.3:p.Lys292Ile
ENST00000378454.7:c.875A>T ENSP00000367715.3:p.Lys292Ile
NM_001195610.1:c.875A>T NP_001182539.1:p.Lys292Ile
NM_016356.4:c.875A>T NP_057440.2:p.Lys292Ile
NM_016356.5:c.875A>T MANE Select NP_057440.2:p.Lys292Ile
NM_001195610.2:c.875A>T NP_001182539.1:p.Lys292Ile
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