Canonical Allele Identifier: CA269648820
Gene: DLL4 HGNC NCBI

Linked Data

dbSNP Id: rs766317657
MyVariant Identifiers: chr15:g.40931806C>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40931806C>A , CM000677.2:g.40931806C>A GRCh38
NC_000015.9:g.41224004C>A , CM000677.1:g.41224004C>A GRCh37
NC_000015.8:g.39011296C>A NCBI36
NG_046974.1:g.7474C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000249749.7:c.658+40C>A MANE Select ENSP00000249749.5:n.658+40C>A
ENST00000249749.6:c.658+40C>A ENSP00000249749.5:n.658+40C>A
ENST00000559440.1:n.887+40C>A
NM_019074.3:c.658+40C>A NP_061947.1:n.658+40C>A
NM_019074.4:c.658+40C>A MANE Select NP_061947.1:n.658+40C>A