Canonical Allele Identifier: CA969005622
Gene: DLL4 HGNC NCBI

Linked Data

dbSNP Id: rs1892776641
gnomAD v3: 15-40931933-C-A
gnomAD v4: 15-40931933-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40931933C>A , CM000677.2:g.40931933C>A GRCh38
NC_000015.9:g.41224131C>A , CM000677.1:g.41224131C>A GRCh37
NC_000015.8:g.39011423C>A NCBI36
NG_046974.1:g.7601C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000249749.7:c.658+167C>A MANE Select ENSP00000249749.5:n.658+167C>A
ENST00000249749.6:c.658+167C>A ENSP00000249749.5:n.658+167C>A
ENST00000559440.1:n.887+167C>A
NM_019074.3:c.658+167C>A NP_061947.1:n.658+167C>A
NM_019074.4:c.658+167C>A MANE Select NP_061947.1:n.658+167C>A
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