Canonical Allele Identifier: CA3654759

Gene: DCDC2

Linked Data

• ClinVar Variation Id: 1255459
• ClinVar RCV Id: RCV001661369 ; RCV001661371 ; RCV001661370 ; RCV001673234 ; RCV002073080
• dbSNP Id: rs807703
• ExAC: 6:24302087 G / A
• gnomAD v2: 6-24302087-G-A
• gnomAD v3: 6-24301859-G-A
• gnomAD v4: 6-24301859-G-A
• MyVariant Identifiers: chr6:g.24302087G>A (hg19) ; chr6:g.24301859G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24301859G>A , CM000668.2:g.24301859G>A	GRCh38
NC_000006.11:g.24302087G>A , CM000668.1:g.24302087G>A	GRCh37
NC_000006.10:g.24410066G>A	NCBI36
NG_012829.1:g.61194C>T
NG_012829.2:g.86434C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378454.8:c.426-13C>T MANE Select	ENSP00000367715.3:n.426-13C>T
ENST00000378454.7:c.426-13C>T	ENSP00000367715.3:n.426-13C>T
NM_001195610.1:c.426-13C>T	NP_001182539.1:n.426-13C>T
NM_016356.4:c.426-13C>T	NP_057440.2:n.426-13C>T
NM_016356.5:c.426-13C>T MANE Select	NP_057440.2:n.426-13C>T
NM_001195610.2:c.426-13C>T	NP_001182539.1:n.426-13C>T