Canonical Allele Identifier: CA507662551
Gene: DLL3 HGNC NCBI

Linked Data

gnomAD v4: 19-39507469-T-C
MyVariant Identifiers: chr19:g.39998109T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39507469T>C , CM000681.2:g.39507469T>C GRCh38
NC_000019.9:g.39998109T>C , CM000681.1:g.39998109T>C GRCh37
NC_000019.8:g.44689949T>C NCBI36
NG_008256.1:g.13553T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000356433.10:c.1524T>C MANE Select ENSP00000348810.4:p.Ala508=
ENST00000205143.4:c.1524T>C ENSP00000205143.3:p.Ala508=
ENST00000356433.9:c.1524T>C ENSP00000348810.4:p.Ala508=
NM_016941.3:c.1524T>C NP_058637.1:p.Ala508=
NM_203486.2:c.1524T>C NP_982353.1:p.Ala508=
NM_016941.4:c.1524T>C NP_058637.1:p.Ala508=
NM_203486.3:c.1524T>C MANE Select NP_982353.1:p.Ala508=
Search 100 bp 5'
Search 100 bp 3'