Canonical Allele Identifier: CA269648921

Gene: DLL4

Linked Data

• dbSNP Id: rs143917704
• gnomAD v2: 15-41224092-A-T
• gnomAD v3: 15-40931894-A-T
• gnomAD v4: 15-40931894-A-T
• MyVariant Identifiers: chr15:g.41224092A>T (hg19) ; chr15:g.40931894A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40931894A>T , CM000677.2:g.40931894A>T	GRCh38
NC_000015.9:g.41224092A>T , CM000677.1:g.41224092A>T	GRCh37
NC_000015.8:g.39011384A>T	NCBI36
NG_046974.1:g.7562A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249749.7:c.658+128A>T MANE Select	ENSP00000249749.5:n.658+128A>T
ENST00000249749.6:c.658+128A>T	ENSP00000249749.5:n.658+128A>T
ENST00000559440.1:n.887+128A>T
NM_019074.3:c.658+128A>T	NP_061947.1:n.658+128A>T
NM_019074.4:c.658+128A>T MANE Select	NP_061947.1:n.658+128A>T