Canonical Allele Identifier: CA363277436
Gene: DCDC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.24205255G>C (hg19) chr6:g.24205027G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24205027G>C , CM000668.2:g.24205027G>C GRCh38
NC_000006.11:g.24205255G>C , CM000668.1:g.24205255G>C GRCh37
NC_000006.10:g.24313234G>C NCBI36
NG_012829.1:g.158026C>G
NG_012829.2:g.183266C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.998C>G MANE Select ENSP00000367715.3:p.Thr333Ser
ENST00000378450.6:c.257C>G ENSP00000367711.3:p.Thr86Ser
ENST00000378454.7:c.998C>G ENSP00000367715.3:p.Thr333Ser
NM_001195610.1:c.998C>G NP_001182539.1:p.Thr333Ser
NM_016356.4:c.998C>G NP_057440.2:p.Thr333Ser
NM_016356.5:c.998C>G MANE Select NP_057440.2:p.Thr333Ser
NM_001195610.2:c.998C>G NP_001182539.1:p.Thr333Ser
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