Canonical Allele Identifier: CA489781793

Gene: DLL4

Linked Data

• dbSNP Id: rs1938552186
• MyVariant Identifiers: chr15:g.41223930C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40931732C>T , CM000677.2:g.40931732C>T	GRCh38
NC_000015.9:g.41223930C>T , CM000677.1:g.41223930C>T	GRCh37
NC_000015.8:g.39011222C>T	NCBI36
NG_046974.1:g.7400C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249749.7:c.624C>T MANE Select	ENSP00000249749.5:p.Cys208=
ENST00000249749.6:c.624C>T	ENSP00000249749.5:p.Cys208=
ENST00000559440.1:n.853C>T
NM_019074.3:c.624C>T	NP_061947.1:p.Cys208=
NM_019074.4:c.624C>T MANE Select	NP_061947.1:p.Cys208=