Canonical Allele Identifier: CA363280790
Gene: DCDC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24291071T>A , CM000668.2:g.24291071T>A GRCh38
NC_000006.11:g.24291299T>A , CM000668.1:g.24291299T>A GRCh37
NC_000006.10:g.24399278T>A NCBI36
NG_012829.1:g.71982A>T
NG_012829.2:g.97222A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.565A>T MANE Select ENSP00000367715.3:p.Thr189Ser
ENST00000378454.7:c.565A>T ENSP00000367715.3:p.Thr189Ser
NM_001195610.1:c.565A>T NP_001182539.1:p.Thr189Ser
NM_016356.4:c.565A>T NP_057440.2:p.Thr189Ser
NM_016356.5:c.565A>T MANE Select NP_057440.2:p.Thr189Ser
NM_001195610.2:c.565A>T NP_001182539.1:p.Thr189Ser