Canonical Allele Identifier: CA448963236
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1561878592
gnomAD v4: 6-24178396-A-G
MyVariant Identifiers: chr6:g.24178624A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24178396A>G , CM000668.2:g.24178396A>G GRCh38
NC_000006.11:g.24178624A>G , CM000668.1:g.24178624A>G GRCh37
NC_000006.10:g.24286603A>G NCBI36
NG_012829.1:g.184657T>C
NG_012829.2:g.209897T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.1260T>C MANE Select ENSP00000367715.3:p.Asn420=
ENST00000378450.6:c.519T>C ENSP00000367711.3:p.Asn173=
ENST00000378454.7:c.1260T>C ENSP00000367715.3:p.Asn420=
NM_001195610.1:c.1260T>C NP_001182539.1:p.Asn420=
NM_016356.4:c.1260T>C NP_057440.2:p.Asn420=
NM_016356.5:c.1260T>C MANE Select NP_057440.2:p.Asn420=
NM_001195610.2:c.1260T>C NP_001182539.1:p.Asn420=