Canonical Allele Identifier: CA2172012957
Gene: DLL4 HGNC NCBI

Linked Data

dbSNP Id: rs1892775831
gnomAD v4: 15-40931868-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40931868G>C , CM000677.2:g.40931868G>C GRCh38
NC_000015.9:g.41224066G>C , CM000677.1:g.41224066G>C GRCh37
NC_000015.8:g.39011358G>C NCBI36
NG_046974.1:g.7536G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000249749.7:c.658+102G>C MANE Select ENSP00000249749.5:n.658+102G>C
ENST00000249749.6:c.658+102G>C ENSP00000249749.5:n.658+102G>C
ENST00000559440.1:n.887+102G>C
NM_019074.3:c.658+102G>C NP_061947.1:n.658+102G>C
NM_019074.4:c.658+102G>C MANE Select NP_061947.1:n.658+102G>C
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