Canonical Allele Identifier: CA136634490
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs902140796
gnomAD v2: 6-24278778-G-A
gnomAD v3: 6-24278550-G-A
gnomAD v4: 6-24278550-G-A
MyVariant Identifiers: chr6:g.24278778G>A (hg19) chr6:g.24278550G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24278550G>A , CM000668.2:g.24278550G>A GRCh38
NC_000006.11:g.24278778G>A , CM000668.1:g.24278778G>A GRCh37
NC_000006.10:g.24386757G>A NCBI36
NG_012829.1:g.84503C>T
NG_012829.2:g.109743C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.760-339C>T MANE Select ENSP00000367715.3:n.760-339C>T
ENST00000378454.7:c.760-339C>T ENSP00000367715.3:n.760-339C>T
NM_001195610.1:c.760-339C>T NP_001182539.1:n.760-339C>T
NM_016356.4:c.760-339C>T NP_057440.2:n.760-339C>T
NM_016356.5:c.760-339C>T MANE Select NP_057440.2:n.760-339C>T
NM_001195610.2:c.760-339C>T NP_001182539.1:n.760-339C>T
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