Canonical Allele Identifier: CA136637325
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1002032199
gnomAD v3: 6-24301767-C-T
gnomAD v4: 6-24301767-C-T
MyVariant Identifiers: chr6:g.24301995C>T (hg19) chr6:g.24301767C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24301767C>T , CM000668.2:g.24301767C>T GRCh38
NC_000006.11:g.24301995C>T , CM000668.1:g.24301995C>T GRCh37
NC_000006.10:g.24409974C>T NCBI36
NG_012829.1:g.61286G>A
NG_012829.2:g.86526G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.505G>A MANE Select ENSP00000367715.3:p.Val169Ile
ENST00000378454.7:c.505G>A ENSP00000367715.3:p.Val169Ile
NM_001195610.1:c.505G>A NP_001182539.1:p.Val169Ile
NM_016356.4:c.505G>A NP_057440.2:p.Val169Ile
NM_016356.5:c.505G>A MANE Select NP_057440.2:p.Val169Ile
NM_001195610.2:c.505G>A NP_001182539.1:p.Val169Ile
Search 100 bp 5'
Search 100 bp 3'