Canonical Allele Identifier: CA566225021

Gene: DCDC2

Linked Data

• dbSNP Id: rs898037001
• gnomAD v2: 6-24302333-A-T
• gnomAD v3: 6-24302105-A-T
• gnomAD v4: 6-24302105-A-T
• MyVariant Identifiers: chr6:g.24302333A>T (hg19) ; chr6:g.24302105A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24302105A>T , CM000668.2:g.24302105A>T	GRCh38
NC_000006.11:g.24302333A>T , CM000668.1:g.24302333A>T	GRCh37
NC_000006.10:g.24410312A>T	NCBI36
NG_012829.1:g.60948T>A
NG_012829.2:g.86188T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378454.8:c.349-61T>A MANE Select	ENSP00000367715.3:n.349-61T>A
ENST00000378454.7:c.349-61T>A	ENSP00000367715.3:n.349-61T>A
NM_001195610.1:c.349-61T>A	NP_001182539.1:n.349-61T>A
NM_016356.4:c.349-61T>A	NP_057440.2:n.349-61T>A
NM_016356.5:c.349-61T>A MANE Select	NP_057440.2:n.349-61T>A
NM_001195610.2:c.349-61T>A	NP_001182539.1:n.349-61T>A