Canonical Allele Identifier: CA566225028
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1375821059
gnomAD v2: 6-24302411-T-C
gnomAD v3: 6-24302183-T-C
gnomAD v4: 6-24302183-T-C
MyVariant Identifiers: chr6:g.24302411T>C (hg19) chr6:g.24302183T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24302183T>C , CM000668.2:g.24302183T>C GRCh38
NC_000006.11:g.24302411T>C , CM000668.1:g.24302411T>C GRCh37
NC_000006.10:g.24410390T>C NCBI36
NG_012829.1:g.60870A>G
NG_012829.2:g.86110A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.349-139A>G MANE Select ENSP00000367715.3:n.349-139A>G
ENST00000378454.7:c.349-139A>G ENSP00000367715.3:n.349-139A>G
NM_001195610.1:c.349-139A>G NP_001182539.1:n.349-139A>G
NM_016356.4:c.349-139A>G NP_057440.2:n.349-139A>G
NM_016356.5:c.349-139A>G MANE Select NP_057440.2:n.349-139A>G
NM_001195610.2:c.349-139A>G NP_001182539.1:n.349-139A>G
Search 100 bp 5'
Search 100 bp 3'