Canonical Allele Identifier: CA136642198

Gene: DCDC2

Linked Data

• dbSNP Id: rs550053344
• gnomAD v3: 6-24347838-A-G
• gnomAD v4: 6-24347838-A-G
• MyVariant Identifiers: chr6:g.24348066A>G (hg19) ; chr6:g.24347838A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24347838A>G , CM000668.2:g.24347838A>G	GRCh38
NC_000006.11:g.24348066A>G , CM000668.1:g.24348066A>G	GRCh37
NC_000006.10:g.24456045A>G	NCBI36
NG_012829.1:g.15215T>C
NG_012829.2:g.40455T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000378454.8:c.348+5731T>C MANE Select	ENSP00000367715.3:n.348+5731T>C
ENST00000378454.7:c.348+5731T>C	ENSP00000367715.3:n.348+5731T>C
NM_001195610.1:c.348+5731T>C	NP_001182539.1:n.348+5731T>C
NM_016356.4:c.348+5731T>C	NP_057440.2:n.348+5731T>C
NM_016356.5:c.348+5731T>C MANE Select	NP_057440.2:n.348+5731T>C
NM_001195610.2:c.348+5731T>C	NP_001182539.1:n.348+5731T>C