Canonical Allele Identifier: CA448963282
Gene: DCDC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.24178708C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24178480C>T , CM000668.2:g.24178480C>T GRCh38
NC_000006.11:g.24178708C>T , CM000668.1:g.24178708C>T GRCh37
NC_000006.10:g.24286687C>T NCBI36
NG_012829.1:g.184573G>A
NG_012829.2:g.209813G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.1176G>A MANE Select ENSP00000367715.3:p.Leu392=
ENST00000378450.6:c.435G>A ENSP00000367711.3:p.Leu145=
ENST00000378454.7:c.1176G>A ENSP00000367715.3:p.Leu392=
NM_001195610.1:c.1176G>A NP_001182539.1:p.Leu392=
NM_016356.4:c.1176G>A NP_057440.2:p.Leu392=
NM_016356.5:c.1176G>A MANE Select NP_057440.2:p.Leu392=
NM_001195610.2:c.1176G>A NP_001182539.1:p.Leu392=
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