Canonical Allele Identifier: CA448963050
Gene: DCDC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.24178576A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24178348A>G , CM000668.2:g.24178348A>G GRCh38
NC_000006.11:g.24178576A>G , CM000668.1:g.24178576A>G GRCh37
NC_000006.10:g.24286555A>G NCBI36
NG_012829.1:g.184705T>C
NG_012829.2:g.209945T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.1308T>C MANE Select ENSP00000367715.3:p.Ala436=
ENST00000378450.6:c.567T>C ENSP00000367711.3:p.Ala189=
ENST00000378454.7:c.1308T>C ENSP00000367715.3:p.Ala436=
NM_001195610.1:c.1308T>C NP_001182539.1:p.Ala436=
NM_016356.4:c.1308T>C NP_057440.2:p.Ala436=
NM_016356.5:c.1308T>C MANE Select NP_057440.2:p.Ala436=
NM_001195610.2:c.1308T>C NP_001182539.1:p.Ala436=
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