Canonical Allele Identifier: CA448951169
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs747533733
MyVariant Identifiers: chr6:g.24291177C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24290949C>G , CM000668.2:g.24290949C>G GRCh38
NC_000006.11:g.24291177C>G , CM000668.1:g.24291177C>G GRCh37
NC_000006.10:g.24399156C>G NCBI36
NG_012829.1:g.72104G>C
NG_012829.2:g.97344G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.687G>C MANE Select ENSP00000367715.3:p.Thr229=
ENST00000378454.7:c.687G>C ENSP00000367715.3:p.Thr229=
NM_001195610.1:c.687G>C NP_001182539.1:p.Thr229=
NM_016356.4:c.687G>C NP_057440.2:p.Thr229=
NM_016356.5:c.687G>C MANE Select NP_057440.2:p.Thr229=
NM_001195610.2:c.687G>C NP_001182539.1:p.Thr229=
Search 100 bp 5'
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