Canonical Allele Identifier: CA9432441
Gene: DLL3 HGNC NCBI

Linked Data

ClinVar Variation Id: 893400
ClinVar RCV Id: RCV001131440 RCV001131441 RCV003106125
dbSNP Id: rs773460228
ExAC: 19:39998026 C / G
gnomAD v2: 19-39998026-C-G
gnomAD v3: 19-39507386-C-G
gnomAD v4: 19-39507386-C-G
MyVariant Identifiers: chr19:g.39998026C>G (hg19) chr19:g.39507386C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39507386C>G , CM000681.2:g.39507386C>G GRCh38
NC_000019.9:g.39998026C>G , CM000681.1:g.39998026C>G GRCh37
NC_000019.8:g.44689866C>G NCBI36
NG_008256.1:g.13470C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356433.10:c.1441C>G MANE Select ENSP00000348810.4:p.Pro481Ala
ENST00000205143.4:c.1441C>G ENSP00000205143.3:p.Pro481Ala
ENST00000356433.9:c.1441C>G ENSP00000348810.4:p.Pro481Ala
NM_016941.3:c.1441C>G NP_058637.1:p.Pro481Ala
NM_203486.2:c.1441C>G NP_982353.1:p.Pro481Ala
NM_016941.4:c.1441C>G NP_058637.1:p.Pro481Ala
NM_203486.3:c.1441C>G MANE Select NP_982353.1:p.Pro481Ala
Search 100 bp 5'
Search 100 bp 3'