Canonical Allele Identifier: CA363280335
Gene: DCDC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.24291202C>G (hg19) chr6:g.24290974C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24290974C>G , CM000668.2:g.24290974C>G GRCh38
NC_000006.11:g.24291202C>G , CM000668.1:g.24291202C>G GRCh37
NC_000006.10:g.24399181C>G NCBI36
NG_012829.1:g.72079G>C
NG_012829.2:g.97319G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.662G>C MANE Select ENSP00000367715.3:p.Ser221Thr
ENST00000378454.7:c.662G>C ENSP00000367715.3:p.Ser221Thr
NM_001195610.1:c.662G>C NP_001182539.1:p.Ser221Thr
NM_016356.4:c.662G>C NP_057440.2:p.Ser221Thr
NM_016356.5:c.662G>C MANE Select NP_057440.2:p.Ser221Thr
NM_001195610.2:c.662G>C NP_001182539.1:p.Ser221Thr
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