Canonical Allele Identifier: CA566222969
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1175650844
gnomAD v2: 6-24290956-C-A
gnomAD v3: 6-24290728-C-A
gnomAD v4: 6-24290728-C-A
MyVariant Identifiers: chr6:g.24290956C>A (hg19) chr6:g.24290728C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24290728C>A , CM000668.2:g.24290728C>A GRCh38
NC_000006.11:g.24290956C>A , CM000668.1:g.24290956C>A GRCh37
NC_000006.10:g.24398935C>A NCBI36
NG_012829.1:g.72325G>T
NG_012829.2:g.97565G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.704+204G>T MANE Select ENSP00000367715.3:n.704+204G>T
ENST00000378454.7:c.704+204G>T ENSP00000367715.3:n.704+204G>T
NM_001195610.1:c.704+204G>T NP_001182539.1:n.704+204G>T
NM_016356.4:c.704+204G>T NP_057440.2:n.704+204G>T
NM_016356.5:c.704+204G>T MANE Select NP_057440.2:n.704+204G>T
NM_001195610.2:c.704+204G>T NP_001182539.1:n.704+204G>T
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