Canonical Allele Identifier: CA507662390

Gene: DLL3

Linked Data

• dbSNP Id: rs1403647985
• gnomAD v4: 19-39507394-C-T
• MyVariant Identifiers: chr19:g.39998034C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39507394C>T , CM000681.2:g.39507394C>T	GRCh38
NC_000019.9:g.39998034C>T , CM000681.1:g.39998034C>T	GRCh37
NC_000019.8:g.44689874C>T	NCBI36
NG_008256.1:g.13478C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356433.10:c.1449C>T MANE Select	ENSP00000348810.4:p.Leu483=
ENST00000205143.4:c.1449C>T	ENSP00000205143.3:p.Leu483=
ENST00000356433.9:c.1449C>T	ENSP00000348810.4:p.Leu483=
NM_016941.3:c.1449C>T	NP_058637.1:p.Leu483=
NM_203486.2:c.1449C>T	NP_982353.1:p.Leu483=
NM_016941.4:c.1449C>T	NP_058637.1:p.Leu483=
NM_203486.3:c.1449C>T MANE Select	NP_982353.1:p.Leu483=