Canonical Allele Identifier: CA7487709
Gene: DLL4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1916133
ClinVar RCV Id: RCV002594355
dbSNP Id: rs138390086
ExAC: 15:41223901 G / A
gnomAD v2: 15-41223901-G-A
gnomAD v3: 15-40931703-G-A
gnomAD v4: 15-40931703-G-A
MyVariant Identifiers: chr15:g.41223901G>A (hg19) chr15:g.40931703G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40931703G>A , CM000677.2:g.40931703G>A GRCh38
NC_000015.9:g.41223901G>A , CM000677.1:g.41223901G>A GRCh37
NC_000015.8:g.39011193G>A NCBI36
NG_046974.1:g.7371G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000249749.7:c.595G>A MANE Select ENSP00000249749.5:p.Val199Met
ENST00000249749.6:c.595G>A ENSP00000249749.5:p.Val199Met
ENST00000559440.1:n.824G>A
NM_019074.3:c.595G>A NP_061947.1:p.Val199Met
NM_019074.4:c.595G>A MANE Select NP_061947.1:p.Val199Met
Search 100 bp 5'
Search 100 bp 3'