Canonical Allele Identifier: CA617558724
Gene: DLL4 HGNC NCBI

Linked Data

dbSNP Id: rs1406322475
gnomAD v2: 15-41224266-G-A
gnomAD v4: 15-40932068-G-A
MyVariant Identifiers: chr15:g.41224266G>A (hg19) chr15:g.40932068G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40932068G>A , CM000677.2:g.40932068G>A GRCh38
NC_000015.9:g.41224266G>A , CM000677.1:g.41224266G>A GRCh37
NC_000015.8:g.39011558G>A NCBI36
NG_046974.1:g.7736G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000249749.7:c.659-103G>A MANE Select ENSP00000249749.5:n.659-103G>A
ENST00000249749.6:c.659-103G>A ENSP00000249749.5:n.659-103G>A
ENST00000559440.1:n.888-103G>A
NM_019074.3:c.659-103G>A NP_061947.1:n.659-103G>A
NM_019074.4:c.659-103G>A MANE Select NP_061947.1:n.659-103G>A
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