Canonical Allele Identifier: CA136625639

Gene: DCDC2

Linked Data

• dbSNP Id: rs1000900227
• gnomAD v3: 6-24204594-G-A
• gnomAD v4: 6-24204594-G-A
• MyVariant Identifiers: chr6:g.24204822G>A (hg19) ; chr6:g.24204594G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24204594G>A , CM000668.2:g.24204594G>A	GRCh38
NC_000006.11:g.24204822G>A , CM000668.1:g.24204822G>A	GRCh37
NC_000006.10:g.24312801G>A	NCBI36
NG_012829.1:g.158459C>T
NG_012829.2:g.183699C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378454.8:c.1023+408C>T MANE Select	ENSP00000367715.3:n.1023+408C>T
ENST00000378450.6:c.282+408C>T	ENSP00000367711.3:n.282+408C>T
ENST00000378454.7:c.1023+408C>T	ENSP00000367715.3:n.1023+408C>T
NM_001195610.1:c.1023+408C>T	NP_001182539.1:n.1023+408C>T
NM_016356.4:c.1023+408C>T	NP_057440.2:n.1023+408C>T
NM_016356.5:c.1023+408C>T MANE Select	NP_057440.2:n.1023+408C>T
NM_001195610.2:c.1023+408C>T	NP_001182539.1:n.1023+408C>T