Canonical Allele Identifier: CA391807075
Gene: DLL4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.41223890T>C (hg19) chr15:g.40931692T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40931692T>C , CM000677.2:g.40931692T>C GRCh38
NC_000015.9:g.41223890T>C , CM000677.1:g.41223890T>C GRCh37
NC_000015.8:g.39011182T>C NCBI36
NG_046974.1:g.7360T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000249749.7:c.584T>C MANE Select ENSP00000249749.5:p.Phe195Ser
ENST00000249749.6:c.584T>C ENSP00000249749.5:p.Phe195Ser
ENST00000559440.1:n.813T>C
NM_019074.3:c.584T>C NP_061947.1:p.Phe195Ser
NM_019074.4:c.584T>C MANE Select NP_061947.1:p.Phe195Ser
Search 100 bp 5'
Search 100 bp 3'