Canonical Allele Identifier: CA405788683
Gene: DLL3 HGNC NCBI

Linked Data

gnomAD v4: 19-39507356-G-T
MyVariant Identifiers: chr19:g.39997996G>T (hg19) chr19:g.39507356G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39507356G>T , CM000681.2:g.39507356G>T GRCh38
NC_000019.9:g.39997996G>T , CM000681.1:g.39997996G>T GRCh37
NC_000019.8:g.44689836G>T NCBI36
NG_008256.1:g.13440G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000356433.10:c.1411G>T MANE Select ENSP00000348810.4:p.Asp471Tyr
ENST00000205143.4:c.1411G>T ENSP00000205143.3:p.Asp471Tyr
ENST00000356433.9:c.1411G>T ENSP00000348810.4:p.Asp471Tyr
NM_016941.3:c.1411G>T NP_058637.1:p.Asp471Tyr
NM_203486.2:c.1411G>T NP_982353.1:p.Asp471Tyr
NM_016941.4:c.1411G>T NP_058637.1:p.Asp471Tyr
NM_203486.3:c.1411G>T MANE Select NP_982353.1:p.Asp471Tyr
Search 100 bp 5'
Search 100 bp 3'