Canonical Allele Identifier: CA136636003
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs113161276
MyVariant Identifiers: chr6:g.24290990T>C (hg19) chr6:g.24290762T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24290762T>C , CM000668.2:g.24290762T>C GRCh38
NC_000006.11:g.24290990T>C , CM000668.1:g.24290990T>C GRCh37
NC_000006.10:g.24398969T>C NCBI36
NG_012829.1:g.72291A>G
NG_012829.2:g.97531A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.704+170A>G MANE Select ENSP00000367715.3:n.704+170A>G
ENST00000378454.7:c.704+170A>G ENSP00000367715.3:n.704+170A>G
NM_001195610.1:c.704+170A>G NP_001182539.1:n.704+170A>G
NM_016356.4:c.704+170A>G NP_057440.2:n.704+170A>G
NM_016356.5:c.704+170A>G MANE Select NP_057440.2:n.704+170A>G
NM_001195610.2:c.704+170A>G NP_001182539.1:n.704+170A>G
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