Canonical Allele Identifier: CA269649036
Gene: DLL4 HGNC NCBI

Linked Data

dbSNP Id: rs959382452
gnomAD v3: 15-40931964-C-G
gnomAD v4: 15-40931964-C-G
MyVariant Identifiers: chr15:g.41224162C>G (hg19) chr15:g.40931964C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40931964C>G , CM000677.2:g.40931964C>G GRCh38
NC_000015.9:g.41224162C>G , CM000677.1:g.41224162C>G GRCh37
NC_000015.8:g.39011454C>G NCBI36
NG_046974.1:g.7632C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000249749.7:c.658+198C>G MANE Select ENSP00000249749.5:n.658+198C>G
ENST00000249749.6:c.658+198C>G ENSP00000249749.5:n.658+198C>G
ENST00000559440.1:n.887+198C>G
NM_019074.3:c.658+198C>G NP_061947.1:n.658+198C>G
NM_019074.4:c.658+198C>G MANE Select NP_061947.1:n.658+198C>G
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