Canonical Allele Identifier: CA448951358

Gene: DCDC2

Linked Data

• dbSNP Id: rs1759379922
• gnomAD v4: 6-24301777-C-T
• MyVariant Identifiers: chr6:g.24302005C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24301777C>T , CM000668.2:g.24301777C>T	GRCh38
NC_000006.11:g.24302005C>T , CM000668.1:g.24302005C>T	GRCh37
NC_000006.10:g.24409984C>T	NCBI36
NG_012829.1:g.61276G>A
NG_012829.2:g.86516G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378454.8:c.495G>A MANE Select	ENSP00000367715.3:p.Gln165=
ENST00000378454.7:c.495G>A	ENSP00000367715.3:p.Gln165=
NM_001195610.1:c.495G>A	NP_001182539.1:p.Gln165=
NM_016356.4:c.495G>A	NP_057440.2:p.Gln165=
NM_016356.5:c.495G>A MANE Select	NP_057440.2:p.Gln165=
NM_001195610.2:c.495G>A	NP_001182539.1:p.Gln165=