Canonical Allele Identifier: CA3654773
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs199553643
ExAC: 6:24302174 A / C
gnomAD v2: 6-24302174-A-C
gnomAD v4: 6-24301946-A-C
MyVariant Identifiers: chr6:g.24302174A>C (hg19) chr6:g.24301946A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24301946A>C , CM000668.2:g.24301946A>C GRCh38
NC_000006.11:g.24302174A>C , CM000668.1:g.24302174A>C GRCh37
NC_000006.10:g.24410153A>C NCBI36
NG_012829.1:g.61107T>G
NG_012829.2:g.86347T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.425+22T>G MANE Select ENSP00000367715.3:n.425+22T>G
ENST00000378454.7:c.425+22T>G ENSP00000367715.3:n.425+22T>G
NM_001195610.1:c.425+22T>G NP_001182539.1:n.425+22T>G
NM_016356.4:c.425+22T>G NP_057440.2:n.425+22T>G
NM_016356.5:c.425+22T>G MANE Select NP_057440.2:n.425+22T>G
NM_001195610.2:c.425+22T>G NP_001182539.1:n.425+22T>G
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