Canonical Allele Identifier: CA308227752
Gene: DLL3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1430619
ClinVar RCV Id: RCV001952487
dbSNP Id: rs111556824
gnomAD v2: 19-39998098-G-A
gnomAD v3: 19-39507458-G-A
gnomAD v4: 19-39507458-G-A
MyVariant Identifiers: chr19:g.39998098G>A (hg19) chr19:g.39507458G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39507458G>A , CM000681.2:g.39507458G>A GRCh38
NC_000019.9:g.39998098G>A , CM000681.1:g.39998098G>A GRCh37
NC_000019.8:g.44689938G>A NCBI36
NG_008256.1:g.13542G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000356433.10:c.1513G>A MANE Select ENSP00000348810.4:p.Val505Met
ENST00000205143.4:c.1513G>A ENSP00000205143.3:p.Val505Met
ENST00000356433.9:c.1513G>A ENSP00000348810.4:p.Val505Met
NM_016941.3:c.1513G>A NP_058637.1:p.Val505Met
NM_203486.2:c.1513G>A NP_982353.1:p.Val505Met
NM_016941.4:c.1513G>A NP_058637.1:p.Val505Met
NM_203486.3:c.1513G>A MANE Select NP_982353.1:p.Val505Met
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