Canonical Allele Identifier: CA269648864
Gene: DLL4 HGNC NCBI

Linked Data

dbSNP Id: rs561334658
gnomAD v2: 15-41224059-G-T
gnomAD v3: 15-40931861-G-T
gnomAD v4: 15-40931861-G-T
MyVariant Identifiers: chr15:g.41224059G>T (hg19) chr15:g.40931861G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40931861G>T , CM000677.2:g.40931861G>T GRCh38
NC_000015.9:g.41224059G>T , CM000677.1:g.41224059G>T GRCh37
NC_000015.8:g.39011351G>T NCBI36
NG_046974.1:g.7529G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000249749.7:c.658+95G>T MANE Select ENSP00000249749.5:n.658+95G>T
ENST00000249749.6:c.658+95G>T ENSP00000249749.5:n.658+95G>T
ENST00000559440.1:n.887+95G>T
NM_019074.3:c.658+95G>T NP_061947.1:n.658+95G>T
NM_019074.4:c.658+95G>T MANE Select NP_061947.1:n.658+95G>T
Search 100 bp 5'
Search 100 bp 3'