Canonical Allele Identifier: CA2172012919
Gene: DLL4 HGNC NCBI

Linked Data

dbSNP Id: rs1892774867
gnomAD v4: 15-40931790-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40931790T>G , CM000677.2:g.40931790T>G GRCh38
NC_000015.9:g.41223988T>G , CM000677.1:g.41223988T>G GRCh37
NC_000015.8:g.39011280T>G NCBI36
NG_046974.1:g.7458T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000249749.7:c.658+24T>G MANE Select ENSP00000249749.5:n.658+24T>G
ENST00000249749.6:c.658+24T>G ENSP00000249749.5:n.658+24T>G
ENST00000559440.1:n.887+24T>G
NM_019074.3:c.658+24T>G NP_061947.1:n.658+24T>G
NM_019074.4:c.658+24T>G MANE Select NP_061947.1:n.658+24T>G
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