Canonical Allele Identifier: CA448951400
Gene: DCDC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.24302074G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24301846G>A , CM000668.2:g.24301846G>A GRCh38
NC_000006.11:g.24302074G>A , CM000668.1:g.24302074G>A GRCh37
NC_000006.10:g.24410053G>A NCBI36
NG_012829.1:g.61207C>T
NG_012829.2:g.86447C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.426C>T MANE Select ENSP00000367715.3:p.Phe142=
ENST00000378454.7:c.426C>T ENSP00000367715.3:p.Phe142=
NM_001195610.1:c.426C>T NP_001182539.1:p.Phe142=
NM_016356.4:c.426C>T NP_057440.2:p.Phe142=
NM_016356.5:c.426C>T MANE Select NP_057440.2:p.Phe142=
NM_001195610.2:c.426C>T NP_001182539.1:p.Phe142=