Canonical Allele Identifier: CA507662546
Gene: DLL3 HGNC NCBI

Linked Data

gnomAD v4: 19-39507466-C-G
MyVariant Identifiers: chr19:g.39998106C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39507466C>G , CM000681.2:g.39507466C>G GRCh38
NC_000019.9:g.39998106C>G , CM000681.1:g.39998106C>G GRCh37
NC_000019.8:g.44689946C>G NCBI36
NG_008256.1:g.13550C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000356433.10:c.1521C>G MANE Select ENSP00000348810.4:p.Gly507=
ENST00000205143.4:c.1521C>G ENSP00000205143.3:p.Gly507=
ENST00000356433.9:c.1521C>G ENSP00000348810.4:p.Gly507=
NM_016941.3:c.1521C>G NP_058637.1:p.Gly507=
NM_203486.2:c.1521C>G NP_982353.1:p.Gly507=
NM_016941.4:c.1521C>G NP_058637.1:p.Gly507=
NM_203486.3:c.1521C>G MANE Select NP_982353.1:p.Gly507=
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