Canonical Allele Identifier: CA269649042
Gene: DLL4 HGNC NCBI

Linked Data

dbSNP Id: rs926497932
gnomAD v3: 15-40931971-C-A
gnomAD v4: 15-40931971-C-A
MyVariant Identifiers: chr15:g.41224169C>A (hg19) chr15:g.40931971C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40931971C>A , CM000677.2:g.40931971C>A GRCh38
NC_000015.9:g.41224169C>A , CM000677.1:g.41224169C>A GRCh37
NC_000015.8:g.39011461C>A NCBI36
NG_046974.1:g.7639C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000249749.7:c.659-200C>A MANE Select ENSP00000249749.5:n.659-200C>A
ENST00000249749.6:c.659-200C>A ENSP00000249749.5:n.659-200C>A
ENST00000559440.1:n.888-200C>A
NM_019074.3:c.659-200C>A NP_061947.1:n.659-200C>A
NM_019074.4:c.659-200C>A MANE Select NP_061947.1:n.659-200C>A
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