Canonical Allele Identifier: CA363280885
Gene: DCDC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1687593
ClinVar RCV Id: RCV002251275
dbSNP Id: rs763299947
MyVariant Identifiers: chr6:g.24301942C>A (hg19) chr6:g.24301714C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24301714C>A , CM000668.2:g.24301714C>A GRCh38
NC_000006.11:g.24301942C>A , CM000668.1:g.24301942C>A GRCh37
NC_000006.10:g.24409921C>A NCBI36
NG_012829.1:g.61339G>T
NG_012829.2:g.86579G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.557+1G>T MANE Select ENSP00000367715.3:n.557+1G>T
ENST00000378454.7:c.557+1G>T ENSP00000367715.3:n.557+1G>T
NM_001195610.1:c.557+1G>T NP_001182539.1:n.557+1G>T
NM_016356.4:c.557+1G>T NP_057440.2:n.557+1G>T
NM_016356.5:c.557+1G>T MANE Select NP_057440.2:n.557+1G>T
NM_001195610.2:c.557+1G>T NP_001182539.1:n.557+1G>T
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