Canonical Allele Identifier: CA136625640

Gene: DCDC2

Linked Data

• dbSNP Id: rs1023037107
• gnomAD v2: 6-24204829-A-C
• gnomAD v3: 6-24204601-A-C
• gnomAD v4: 6-24204601-A-C
• MyVariant Identifiers: chr6:g.24204829A>C (hg19) ; chr6:g.24204601A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24204601A>C , CM000668.2:g.24204601A>C	GRCh38
NC_000006.11:g.24204829A>C , CM000668.1:g.24204829A>C	GRCh37
NC_000006.10:g.24312808A>C	NCBI36
NG_012829.1:g.158452T>G
NG_012829.2:g.183692T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378454.8:c.1023+401T>G MANE Select	ENSP00000367715.3:n.1023+401T>G
ENST00000378450.6:c.282+401T>G	ENSP00000367711.3:n.282+401T>G
ENST00000378454.7:c.1023+401T>G	ENSP00000367715.3:n.1023+401T>G
NM_001195610.1:c.1023+401T>G	NP_001182539.1:n.1023+401T>G
NM_016356.4:c.1023+401T>G	NP_057440.2:n.1023+401T>G
NM_016356.5:c.1023+401T>G MANE Select	NP_057440.2:n.1023+401T>G
NM_001195610.2:c.1023+401T>G	NP_001182539.1:n.1023+401T>G