Canonical Allele Identifier: CA136637329
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1014857709
MyVariant Identifiers: chr6:g.24302119A>C (hg19) chr6:g.24301891A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24301891A>C , CM000668.2:g.24301891A>C GRCh38
NC_000006.11:g.24302119A>C , CM000668.1:g.24302119A>C GRCh37
NC_000006.10:g.24410098A>C NCBI36
NG_012829.1:g.61162T>G
NG_012829.2:g.86402T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.426-45T>G MANE Select ENSP00000367715.3:n.426-45T>G
ENST00000378454.7:c.426-45T>G ENSP00000367715.3:n.426-45T>G
NM_001195610.1:c.426-45T>G NP_001182539.1:n.426-45T>G
NM_016356.4:c.426-45T>G NP_057440.2:n.426-45T>G
NM_016356.5:c.426-45T>G MANE Select NP_057440.2:n.426-45T>G
NM_001195610.2:c.426-45T>G NP_001182539.1:n.426-45T>G
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