Canonical Allele Identifier: CA363281012
Gene: DCDC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3080428
ClinVar RCV Id: RCV004373255
MyVariant Identifiers: chr6:g.24302001C>A (hg19) chr6:g.24301773C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24301773C>A , CM000668.2:g.24301773C>A GRCh38
NC_000006.11:g.24302001C>A , CM000668.1:g.24302001C>A GRCh37
NC_000006.10:g.24409980C>A NCBI36
NG_012829.1:g.61280G>T
NG_012829.2:g.86520G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.499G>T MANE Select ENSP00000367715.3:p.Asp167Tyr
ENST00000378454.7:c.499G>T ENSP00000367715.3:p.Asp167Tyr
NM_001195610.1:c.499G>T NP_001182539.1:p.Asp167Tyr
NM_016356.4:c.499G>T NP_057440.2:p.Asp167Tyr
NM_016356.5:c.499G>T MANE Select NP_057440.2:p.Asp167Tyr
NM_001195610.2:c.499G>T NP_001182539.1:p.Asp167Tyr
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