Canonical Allele Identifier: CA363277971
Gene: DCDC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.24278327A>T (hg19) chr6:g.24278099A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24278099A>T , CM000668.2:g.24278099A>T GRCh38
NC_000006.11:g.24278327A>T , CM000668.1:g.24278327A>T GRCh37
NC_000006.10:g.24386306A>T NCBI36
NG_012829.1:g.84954T>A
NG_012829.2:g.110194T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.872T>A MANE Select ENSP00000367715.3:p.Leu291Ter
ENST00000378454.7:c.872T>A ENSP00000367715.3:p.Leu291Ter
NM_001195610.1:c.872T>A NP_001182539.1:p.Leu291Ter
NM_016356.4:c.872T>A NP_057440.2:p.Leu291Ter
NM_016356.5:c.872T>A MANE Select NP_057440.2:p.Leu291Ter
NM_001195610.2:c.872T>A NP_001182539.1:p.Leu291Ter
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