Canonical Allele Identifier: CA363281177

Gene: DCDC2

Linked Data

• ClinVar Variation Id: 1492885
• ClinVar RCV Id: RCV002012513
• dbSNP Id: rs2113838226
• MyVariant Identifiers: chr6:g.24302076T>C (hg19) ; chr6:g.24301848T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24301848T>C , CM000668.2:g.24301848T>C	GRCh38
NC_000006.11:g.24302076T>C , CM000668.1:g.24302076T>C	GRCh37
NC_000006.10:g.24410055T>C	NCBI36
NG_012829.1:g.61205A>G
NG_012829.2:g.86445A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378454.8:c.426-2A>G MANE Select	ENSP00000367715.3:n.426-2A>G
ENST00000378454.7:c.426-2A>G	ENSP00000367715.3:n.426-2A>G
NM_001195610.1:c.426-2A>G	NP_001182539.1:n.426-2A>G
NM_016356.4:c.426-2A>G	NP_057440.2:n.426-2A>G
NM_016356.5:c.426-2A>G MANE Select	NP_057440.2:n.426-2A>G
NM_001195610.2:c.426-2A>G	NP_001182539.1:n.426-2A>G