Canonical Allele Identifier: CA136622211
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs143521294
gnomAD v2: 6-24178671-T-C
gnomAD v3: 6-24178443-T-C
gnomAD v4: 6-24178443-T-C
MyVariant Identifiers: chr6:g.24178671T>C (hg19) chr6:g.24178443T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24178443T>C , CM000668.2:g.24178443T>C GRCh38
NC_000006.11:g.24178671T>C , CM000668.1:g.24178671T>C GRCh37
NC_000006.10:g.24286650T>C NCBI36
NG_012829.1:g.184610A>G
NG_012829.2:g.209850A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.1213A>G MANE Select ENSP00000367715.3:p.Asn405Asp
ENST00000378450.6:c.472A>G ENSP00000367711.3:p.Asn158Asp
ENST00000378454.7:c.1213A>G ENSP00000367715.3:p.Asn405Asp
NM_001195610.1:c.1213A>G NP_001182539.1:p.Asn405Asp
NM_016356.4:c.1213A>G NP_057440.2:p.Asn405Asp
NM_016356.5:c.1213A>G MANE Select NP_057440.2:p.Asn405Asp
NM_001195610.2:c.1213A>G NP_001182539.1:p.Asn405Asp
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