Canonical Allele Identifier: CA363280338
Gene: DCDC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24290975T>G , CM000668.2:g.24290975T>G GRCh38
NC_000006.11:g.24291203T>G , CM000668.1:g.24291203T>G GRCh37
NC_000006.10:g.24399182T>G NCBI36
NG_012829.1:g.72078A>C
NG_012829.2:g.97318A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.661A>C MANE Select ENSP00000367715.3:p.Ser221Arg
ENST00000378454.7:c.661A>C ENSP00000367715.3:p.Ser221Arg
NM_001195610.1:c.661A>C NP_001182539.1:p.Ser221Arg
NM_016356.4:c.661A>C NP_057440.2:p.Ser221Arg
NM_016356.5:c.661A>C MANE Select NP_057440.2:p.Ser221Arg
NM_001195610.2:c.661A>C NP_001182539.1:p.Ser221Arg