Canonical Allele Identifier: CA363281151
Gene: DCDC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.24302066G>A (hg19) chr6:g.24301838G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24301838G>A , CM000668.2:g.24301838G>A GRCh38
NC_000006.11:g.24302066G>A , CM000668.1:g.24302066G>A GRCh37
NC_000006.10:g.24410045G>A NCBI36
NG_012829.1:g.61215C>T
NG_012829.2:g.86455C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.434C>T MANE Select ENSP00000367715.3:p.Ala145Val
ENST00000378454.7:c.434C>T ENSP00000367715.3:p.Ala145Val
NM_001195610.1:c.434C>T NP_001182539.1:p.Ala145Val
NM_016356.4:c.434C>T NP_057440.2:p.Ala145Val
NM_016356.5:c.434C>T MANE Select NP_057440.2:p.Ala145Val
NM_001195610.2:c.434C>T NP_001182539.1:p.Ala145Val
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