Canonical Allele Identifier: CA269648952

Gene: DLL4

Linked Data

• dbSNP Id: rs528331019
• gnomAD v2: 15-41224126-C-G
• gnomAD v3: 15-40931928-C-G
• gnomAD v4: 15-40931928-C-G
• MyVariant Identifiers: chr15:g.41224126C>G (hg19) ; chr15:g.40931928C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40931928C>G , CM000677.2:g.40931928C>G	GRCh38
NC_000015.9:g.41224126C>G , CM000677.1:g.41224126C>G	GRCh37
NC_000015.8:g.39011418C>G	NCBI36
NG_046974.1:g.7596C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249749.7:c.658+162C>G MANE Select	ENSP00000249749.5:n.658+162C>G
ENST00000249749.6:c.658+162C>G	ENSP00000249749.5:n.658+162C>G
ENST00000559440.1:n.887+162C>G
NM_019074.3:c.658+162C>G	NP_061947.1:n.658+162C>G
NM_019074.4:c.658+162C>G MANE Select	NP_061947.1:n.658+162C>G