Canonical Allele Identifier: CA405789166
Gene: DLL3 HGNC NCBI

Linked Data

dbSNP Id: rs1272813407
gnomAD v2: 19-39998105-G-T
gnomAD v3: 19-39507465-G-T
gnomAD v4: 19-39507465-G-T
MyVariant Identifiers: chr19:g.39998105G>T (hg19) chr19:g.39507465G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39507465G>T , CM000681.2:g.39507465G>T GRCh38
NC_000019.9:g.39998105G>T , CM000681.1:g.39998105G>T GRCh37
NC_000019.8:g.44689945G>T NCBI36
NG_008256.1:g.13549G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000356433.10:c.1520G>T MANE Select ENSP00000348810.4:p.Gly507Val
ENST00000205143.4:c.1520G>T ENSP00000205143.3:p.Gly507Val
ENST00000356433.9:c.1520G>T ENSP00000348810.4:p.Gly507Val
NM_016941.3:c.1520G>T NP_058637.1:p.Gly507Val
NM_203486.2:c.1520G>T NP_982353.1:p.Gly507Val
NM_016941.4:c.1520G>T NP_058637.1:p.Gly507Val
NM_203486.3:c.1520G>T MANE Select NP_982353.1:p.Gly507Val
Search 100 bp 5'
Search 100 bp 3'