Canonical Allele Identifier: CA3654460

Gene: DCDC2

Linked Data

• ClinVar Variation Id: 2926257
• ClinVar RCV Id: RCV003786543
• dbSNP Id: rs752452396
• ExAC: 6:24178549 T / C
• gnomAD v2: 6-24178549-T-C
• gnomAD v3: 6-24178321-T-C
• gnomAD v4: 6-24178321-T-C
• MyVariant Identifiers: chr6:g.24178549T>C (hg19) ; chr6:g.24178321T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24178321T>C , CM000668.2:g.24178321T>C	GRCh38
NC_000006.11:g.24178549T>C , CM000668.1:g.24178549T>C	GRCh37
NC_000006.10:g.24286528T>C	NCBI36
NG_012829.1:g.184732A>G
NG_012829.2:g.209972A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000378454.8:c.1326+9A>G MANE Select	ENSP00000367715.3:n.1326+9A>G
ENST00000378450.6:c.585+9A>G	ENSP00000367711.3:n.585+9A>G
ENST00000378454.7:c.1326+9A>G	ENSP00000367715.3:n.1326+9A>G
NM_001195610.1:c.1326+9A>G	NP_001182539.1:n.1326+9A>G
NM_016356.4:c.1326+9A>G	NP_057440.2:n.1326+9A>G
NM_016356.5:c.1326+9A>G MANE Select	NP_057440.2:n.1326+9A>G
NM_001195610.2:c.1326+9A>G	NP_001182539.1:n.1326+9A>G