Canonical Allele Identifier: CA7487696

Gene: DLL4

Linked Data

• dbSNP Id: rs763342333
• ExAC: 15:41223795 C / A
• gnomAD v2: 15-41223795-C-A
• gnomAD v4: 15-40931597-C-A
• MyVariant Identifiers: chr15:g.41223795C>A (hg19) ; chr15:g.40931597C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40931597C>A , CM000677.2:g.40931597C>A	GRCh38
NC_000015.9:g.41223795C>A , CM000677.1:g.41223795C>A	GRCh37
NC_000015.8:g.39011087C>A	NCBI36
NG_046974.1:g.7265C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249749.7:c.489C>A MANE Select	ENSP00000249749.5:p.Thr163=
ENST00000249749.6:c.489C>A	ENSP00000249749.5:p.Thr163=
ENST00000559440.1:n.718C>A
NM_019074.3:c.489C>A	NP_061947.1:p.Thr163=
NM_019074.4:c.489C>A MANE Select	NP_061947.1:p.Thr163=