Canonical Allele Identifier: CA363277435

Gene: DCDC2

Linked Data

• dbSNP Id: rs1239618857
• gnomAD v2: 6-24205255-G-T
• gnomAD v4: 6-24205027-G-T
• MyVariant Identifiers: chr6:g.24205255G>T (hg19) ; chr6:g.24205027G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24205027G>T , CM000668.2:g.24205027G>T	GRCh38
NC_000006.11:g.24205255G>T , CM000668.1:g.24205255G>T	GRCh37
NC_000006.10:g.24313234G>T	NCBI36
NG_012829.1:g.158026C>A
NG_012829.2:g.183266C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000378454.8:c.998C>A MANE Select	ENSP00000367715.3:p.Thr333Asn
ENST00000378450.6:c.257C>A	ENSP00000367711.3:p.Thr86Asn
ENST00000378454.7:c.998C>A	ENSP00000367715.3:p.Thr333Asn
NM_001195610.1:c.998C>A	NP_001182539.1:p.Thr333Asn
NM_016356.4:c.998C>A	NP_057440.2:p.Thr333Asn
NM_016356.5:c.998C>A MANE Select	NP_057440.2:p.Thr333Asn
NM_001195610.2:c.998C>A	NP_001182539.1:p.Thr333Asn