Canonical Allele Identifier: CA448951345
Gene: DCDC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.24301978T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24301750T>A , CM000668.2:g.24301750T>A GRCh38
NC_000006.11:g.24301978T>A , CM000668.1:g.24301978T>A GRCh37
NC_000006.10:g.24409957T>A NCBI36
NG_012829.1:g.61303A>T
NG_012829.2:g.86543A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.522A>T MANE Select ENSP00000367715.3:p.Thr174=
ENST00000378454.7:c.522A>T ENSP00000367715.3:p.Thr174=
NM_001195610.1:c.522A>T NP_001182539.1:p.Thr174=
NM_016356.4:c.522A>T NP_057440.2:p.Thr174=
NM_016356.5:c.522A>T MANE Select NP_057440.2:p.Thr174=
NM_001195610.2:c.522A>T NP_001182539.1:p.Thr174=