Canonical Allele Identifier: CA566291265

Gene: DCDC2

Linked Data

• dbSNP Id: rs1443758881
• gnomAD v2: 6-24278239-A-G
• gnomAD v4: 6-24278011-A-G
• MyVariant Identifiers: chr6:g.24278239A>G (hg19) ; chr6:g.24278011A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24278011A>G , CM000668.2:g.24278011A>G	GRCh38
NC_000006.11:g.24278239A>G , CM000668.1:g.24278239A>G	GRCh37
NC_000006.10:g.24386218A>G	NCBI36
NG_012829.1:g.85042T>C
NG_012829.2:g.110282T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000378454.8:c.922+38T>C MANE Select	ENSP00000367715.3:n.922+38T>C
ENST00000378454.7:c.922+38T>C	ENSP00000367715.3:n.922+38T>C
NM_001195610.1:c.922+38T>C	NP_001182539.1:n.922+38T>C
NM_016356.4:c.922+38T>C	NP_057440.2:n.922+38T>C
NM_016356.5:c.922+38T>C MANE Select	NP_057440.2:n.922+38T>C
NM_001195610.2:c.922+38T>C	NP_001182539.1:n.922+38T>C