Canonical Allele Identifier: CA136622165
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs940944687
gnomAD v3: 6-24177911-G-T
gnomAD v4: 6-24177911-G-T
MyVariant Identifiers: chr6:g.24178139G>T (hg19) chr6:g.24177911G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24177911G>T , CM000668.2:g.24177911G>T GRCh38
NC_000006.11:g.24178139G>T , CM000668.1:g.24178139G>T GRCh37
NC_000006.10:g.24286118G>T NCBI36
NG_012829.1:g.185142C>A
NG_012829.2:g.210382C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.1326+419C>A MANE Select ENSP00000367715.3:n.1326+419C>A
ENST00000378450.6:c.585+419C>A ENSP00000367711.3:n.585+419C>A
ENST00000378454.7:c.1326+419C>A ENSP00000367715.3:n.1326+419C>A
NM_001195610.1:c.1326+419C>A NP_001182539.1:n.1326+419C>A
NM_016356.4:c.1326+419C>A NP_057440.2:n.1326+419C>A
NM_016356.5:c.1326+419C>A MANE Select NP_057440.2:n.1326+419C>A
NM_001195610.2:c.1326+419C>A NP_001182539.1:n.1326+419C>A
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