Canonical Allele Identifier: CA507662459
Gene: DLL3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.39998067T>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39507427T>A , CM000681.2:g.39507427T>A GRCh38
NC_000019.9:g.39998067T>A , CM000681.1:g.39998067T>A GRCh37
NC_000019.8:g.44689907T>A NCBI36
NG_008256.1:g.13511T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356433.10:c.1482T>A MANE Select ENSP00000348810.4:p.Pro494=
ENST00000205143.4:c.1482T>A ENSP00000205143.3:p.Pro494=
ENST00000356433.9:c.1482T>A ENSP00000348810.4:p.Pro494=
NM_016941.3:c.1482T>A NP_058637.1:p.Pro494=
NM_203486.2:c.1482T>A NP_982353.1:p.Pro494=
NM_016941.4:c.1482T>A NP_058637.1:p.Pro494=
NM_203486.3:c.1482T>A MANE Select NP_982353.1:p.Pro494=
Search 100 bp 5'
Search 100 bp 3'