Canonical Allele Identifier: CA363277932
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1181699754
gnomAD v2: 6-24278316-C-T
gnomAD v4: 6-24278088-C-T
MyVariant Identifiers: chr6:g.24278316C>T (hg19) chr6:g.24278088C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24278088C>T , CM000668.2:g.24278088C>T GRCh38
NC_000006.11:g.24278316C>T , CM000668.1:g.24278316C>T GRCh37
NC_000006.10:g.24386295C>T NCBI36
NG_012829.1:g.84965G>A
NG_012829.2:g.110205G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.883G>A MANE Select ENSP00000367715.3:p.Val295Ile
ENST00000378454.7:c.883G>A ENSP00000367715.3:p.Val295Ile
NM_001195610.1:c.883G>A NP_001182539.1:p.Val295Ile
NM_016356.4:c.883G>A NP_057440.2:p.Val295Ile
NM_016356.5:c.883G>A MANE Select NP_057440.2:p.Val295Ile
NM_001195610.2:c.883G>A NP_001182539.1:p.Val295Ile
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