Canonical Allele Identifier: CA363279897
Gene: DCDC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.24178639C>A (hg19) chr6:g.24178411C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24178411C>A , CM000668.2:g.24178411C>A GRCh38
NC_000006.11:g.24178639C>A , CM000668.1:g.24178639C>A GRCh37
NC_000006.10:g.24286618C>A NCBI36
NG_012829.1:g.184642G>T
NG_012829.2:g.209882G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.1245G>T MANE Select ENSP00000367715.3:p.Glu415Asp
ENST00000378450.6:c.504G>T ENSP00000367711.3:p.Glu168Asp
ENST00000378454.7:c.1245G>T ENSP00000367715.3:p.Glu415Asp
NM_001195610.1:c.1245G>T NP_001182539.1:p.Glu415Asp
NM_016356.4:c.1245G>T NP_057440.2:p.Glu415Asp
NM_016356.5:c.1245G>T MANE Select NP_057440.2:p.Glu415Asp
NM_001195610.2:c.1245G>T NP_001182539.1:p.Glu415Asp
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