Canonical Allele Identifier: CA566291296

Gene: DCDC2

Linked Data

• dbSNP Id: rs1488852495
• gnomAD v2: 6-24301894-T-A
• gnomAD v4: 6-24301666-T-A
• MyVariant Identifiers: chr6:g.24301894T>A (hg19) ; chr6:g.24301666T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24301666T>A , CM000668.2:g.24301666T>A	GRCh38
NC_000006.11:g.24301894T>A , CM000668.1:g.24301894T>A	GRCh37
NC_000006.10:g.24409873T>A	NCBI36
NG_012829.1:g.61387A>T
NG_012829.2:g.86627A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000378454.8:c.557+49A>T MANE Select	ENSP00000367715.3:n.557+49A>T
ENST00000378454.7:c.557+49A>T	ENSP00000367715.3:n.557+49A>T
NM_001195610.1:c.557+49A>T	NP_001182539.1:n.557+49A>T
NM_016356.4:c.557+49A>T	NP_057440.2:n.557+49A>T
NM_016356.5:c.557+49A>T MANE Select	NP_057440.2:n.557+49A>T
NM_001195610.2:c.557+49A>T	NP_001182539.1:n.557+49A>T