Canonical Allele Identifier: CA448951276
Gene: DCDC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.24175003T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24174775T>C , CM000668.2:g.24174775T>C GRCh38
NC_000006.11:g.24175003T>C , CM000668.1:g.24175003T>C GRCh37
NC_000006.10:g.24282982T>C NCBI36
NG_012829.1:g.188278A>G
NG_012829.2:g.213518A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.1386A>G MANE Select ENSP00000367715.3:p.Glu462=
ENST00000378450.6:c.645A>G ENSP00000367711.3:p.Glu215=
ENST00000378454.7:c.1386A>G ENSP00000367715.3:p.Glu462=
NM_001195610.1:c.1386A>G NP_001182539.1:p.Glu462=
NM_016356.4:c.1386A>G NP_057440.2:p.Glu462=
NM_016356.5:c.1386A>G MANE Select NP_057440.2:p.Glu462=
NM_001195610.2:c.1386A>G NP_001182539.1:p.Glu462=