Canonical Allele Identifier: CA509661694
Gene: JAG1 HGNC NCBI

Linked Data

gnomAD v4: 20-10650248-T-C
MyVariant Identifiers: chr20:g.10630896T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.10650248T>C , CM000682.2:g.10650248T>C GRCh38
NC_000020.10:g.10630896T>C , CM000682.1:g.10630896T>C GRCh37
NC_000020.9:g.10578896T>C NCBI36
NG_007496.1:g.28799A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000254958.10:c.1233A>G MANE Select ENSP00000254958.4:p.Leu411=
ENST00000617965.2:n.1822A>G
ENST00000254958.9:c.1233A>G ENSP00000254958.4:p.Leu411=
ENST00000423891.6:n.1099A>G
ENST00000622545.1:c.10A>G
NM_000214.2:c.1233A>G NP_000205.1:p.Leu411=
NM_000214.3:c.1233A>G MANE Select NP_000205.1:p.Leu411=
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Search 100 bp 3'