Canonical Allele Identifier: CA507662078
Gene: DLL3 HGNC NCBI

Linked Data

gnomAD v4: 19-39507259-T-C
MyVariant Identifiers: chr19:g.39997899T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39507259T>C , CM000681.2:g.39507259T>C GRCh38
NC_000019.9:g.39997899T>C , CM000681.1:g.39997899T>C GRCh37
NC_000019.8:g.44689739T>C NCBI36
NG_008256.1:g.13343T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356433.10:c.1314T>C MANE Select ENSP00000348810.4:p.Cys438=
ENST00000205143.4:c.1314T>C ENSP00000205143.3:p.Cys438=
ENST00000356433.9:c.1314T>C ENSP00000348810.4:p.Cys438=
ENST00000596614.5:c.630T>C ENSP00000471688.1:p.Cys210=
NM_016941.3:c.1314T>C NP_058637.1:p.Cys438=
NM_203486.2:c.1314T>C NP_982353.1:p.Cys438=
NM_016941.4:c.1314T>C NP_058637.1:p.Cys438=
NM_203486.3:c.1314T>C MANE Select NP_982353.1:p.Cys438=
Search 100 bp 5'
Search 100 bp 3'