Canonical Allele Identifier: CA363280949
Gene: DCDC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24301745T>G , CM000668.2:g.24301745T>G GRCh38
NC_000006.11:g.24301973T>G , CM000668.1:g.24301973T>G GRCh37
NC_000006.10:g.24409952T>G NCBI36
NG_012829.1:g.61308A>C
NG_012829.2:g.86548A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.527A>C MANE Select ENSP00000367715.3:p.Lys176Thr
ENST00000378454.7:c.527A>C ENSP00000367715.3:p.Lys176Thr
NM_001195610.1:c.527A>C NP_001182539.1:p.Lys176Thr
NM_016356.4:c.527A>C NP_057440.2:p.Lys176Thr
NM_016356.5:c.527A>C MANE Select NP_057440.2:p.Lys176Thr
NM_001195610.2:c.527A>C NP_001182539.1:p.Lys176Thr