Canonical Allele Identifier: CA363280219
Gene: DCDC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.24291179T>G (hg19) chr6:g.24290951T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24290951T>G , CM000668.2:g.24290951T>G GRCh38
NC_000006.11:g.24291179T>G , CM000668.1:g.24291179T>G GRCh37
NC_000006.10:g.24399158T>G NCBI36
NG_012829.1:g.72102A>C
NG_012829.2:g.97342A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.685A>C MANE Select ENSP00000367715.3:p.Thr229Pro
ENST00000378454.7:c.685A>C ENSP00000367715.3:p.Thr229Pro
NM_001195610.1:c.685A>C NP_001182539.1:p.Thr229Pro
NM_016356.4:c.685A>C NP_057440.2:p.Thr229Pro
NM_016356.5:c.685A>C MANE Select NP_057440.2:p.Thr229Pro
NM_001195610.2:c.685A>C NP_001182539.1:p.Thr229Pro
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