Canonical Allele Identifier: CA7487721
Gene: DLL4 HGNC NCBI

Linked Data

dbSNP Id: rs750399275
ExAC: 15:41224002 G / T
gnomAD v2: 15-41224002-G-T
gnomAD v4: 15-40931804-G-T
MyVariant Identifiers: chr15:g.41224002G>T (hg19) chr15:g.40931804G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40931804G>T , CM000677.2:g.40931804G>T GRCh38
NC_000015.9:g.41224002G>T , CM000677.1:g.41224002G>T GRCh37
NC_000015.8:g.39011294G>T NCBI36
NG_046974.1:g.7472G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000249749.7:c.658+38G>T MANE Select ENSP00000249749.5:n.658+38G>T
ENST00000249749.6:c.658+38G>T ENSP00000249749.5:n.658+38G>T
ENST00000559440.1:n.887+38G>T
NM_019074.3:c.658+38G>T NP_061947.1:n.658+38G>T
NM_019074.4:c.658+38G>T MANE Select NP_061947.1:n.658+38G>T
Search 100 bp 5'
Search 100 bp 3'