Canonical Allele Identifier: CA391806866
Gene: DLL4 HGNC NCBI

Linked Data

gnomAD v4: 15-40931599-T-G
MyVariant Identifiers: chr15:g.41223797T>G (hg19) chr15:g.40931599T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40931599T>G , CM000677.2:g.40931599T>G GRCh38
NC_000015.9:g.41223797T>G , CM000677.1:g.41223797T>G GRCh37
NC_000015.8:g.39011089T>G NCBI36
NG_046974.1:g.7267T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000249749.7:c.491T>G MANE Select ENSP00000249749.5:p.Leu164Arg
ENST00000249749.6:c.491T>G ENSP00000249749.5:p.Leu164Arg
ENST00000559440.1:n.720T>G
NM_019074.3:c.491T>G NP_061947.1:p.Leu164Arg
NM_019074.4:c.491T>G MANE Select NP_061947.1:p.Leu164Arg
Search 100 bp 5'
Search 100 bp 3'