Canonical Allele Identifier: CA363281201
Gene: DCDC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24301975T>A , CM000668.2:g.24301975T>A GRCh38
NC_000006.11:g.24302203T>A , CM000668.1:g.24302203T>A GRCh37
NC_000006.10:g.24410182T>A NCBI36
NG_012829.1:g.61078A>T
NG_012829.2:g.86318A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.418A>T MANE Select ENSP00000367715.3:p.Thr140Ser
ENST00000378454.7:c.418A>T ENSP00000367715.3:p.Thr140Ser
NM_001195610.1:c.418A>T NP_001182539.1:p.Thr140Ser
NM_016356.4:c.418A>T NP_057440.2:p.Thr140Ser
NM_016356.5:c.418A>T MANE Select NP_057440.2:p.Thr140Ser
NM_001195610.2:c.418A>T NP_001182539.1:p.Thr140Ser