Canonical Allele Identifier: CA448963255
Gene: DCDC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.24178663G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24178435G>T , CM000668.2:g.24178435G>T GRCh38
NC_000006.11:g.24178663G>T , CM000668.1:g.24178663G>T GRCh37
NC_000006.10:g.24286642G>T NCBI36
NG_012829.1:g.184618C>A
NG_012829.2:g.209858C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.1221C>A MANE Select ENSP00000367715.3:p.Gly407=
ENST00000378450.6:c.480C>A ENSP00000367711.3:p.Gly160=
ENST00000378454.7:c.1221C>A ENSP00000367715.3:p.Gly407=
NM_001195610.1:c.1221C>A NP_001182539.1:p.Gly407=
NM_016356.4:c.1221C>A NP_057440.2:p.Gly407=
NM_016356.5:c.1221C>A MANE Select NP_057440.2:p.Gly407=
NM_001195610.2:c.1221C>A NP_001182539.1:p.Gly407=