Canonical Allele Identifier: CA448950364
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1244680675
gnomAD v2: 6-24278329-T-C
gnomAD v4: 6-24278101-T-C
MyVariant Identifiers: chr6:g.24278329T>C (hg19) chr6:g.24278101T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24278101T>C , CM000668.2:g.24278101T>C GRCh38
NC_000006.11:g.24278329T>C , CM000668.1:g.24278329T>C GRCh37
NC_000006.10:g.24386308T>C NCBI36
NG_012829.1:g.84952A>G
NG_012829.2:g.110192A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.870A>G MANE Select ENSP00000367715.3:p.Lys290=
ENST00000378454.7:c.870A>G ENSP00000367715.3:p.Lys290=
NM_001195610.1:c.870A>G NP_001182539.1:p.Lys290=
NM_016356.4:c.870A>G NP_057440.2:p.Lys290=
NM_016356.5:c.870A>G MANE Select NP_057440.2:p.Lys290=
NM_001195610.2:c.870A>G NP_001182539.1:p.Lys290=
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