Canonical Allele Identifier: CA507662121
Gene: DLL3 HGNC NCBI

Linked Data

dbSNP Id: rs1263220669
gnomAD v3: 19-39507562-A-G
gnomAD v4: 19-39507562-A-G
MyVariant Identifiers: chr19:g.39998202A>G (hg19) chr19:g.39507562A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39507562A>G , CM000681.2:g.39507562A>G GRCh38
NC_000019.9:g.39998202A>G , CM000681.1:g.39998202A>G GRCh37
NC_000019.8:g.44690042A>G NCBI36
NG_008256.1:g.13646A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356433.10:c.1617A>G MANE Select ENSP00000348810.4:p.Ala539=
ENST00000205143.4:c.1617A>G ENSP00000205143.3:p.Ala539=
ENST00000356433.9:c.1617A>G ENSP00000348810.4:p.Ala539=
NM_016941.3:c.1617A>G NP_058637.1:p.Ala539=
NM_203486.2:c.1617A>G NP_982353.1:p.Ala539=
NM_016941.4:c.1617A>G NP_058637.1:p.Ala539=
NM_203486.3:c.1617A>G MANE Select NP_982353.1:p.Ala539=
Search 100 bp 5'
Search 100 bp 3'