Canonical Allele Identifier: CA2172012951
Gene: DLL4 HGNC NCBI

Linked Data

dbSNP Id: rs1892775693

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40931852T>A , CM000677.2:g.40931852T>A GRCh38
NC_000015.9:g.41224050T>A , CM000677.1:g.41224050T>A GRCh37
NC_000015.8:g.39011342T>A NCBI36
NG_046974.1:g.7520T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000249749.7:c.658+86T>A MANE Select ENSP00000249749.5:n.658+86T>A
ENST00000249749.6:c.658+86T>A ENSP00000249749.5:n.658+86T>A
ENST00000559440.1:n.887+86T>A
NM_019074.3:c.658+86T>A NP_061947.1:n.658+86T>A
NM_019074.4:c.658+86T>A MANE Select NP_061947.1:n.658+86T>A