Canonical Allele Identifier: CA9764230

Gene: JAG1

Linked Data

• ClinVar Variation Id: 337747
• ClinVar RCV Id: RCV000281669 ; RCV001497922 ; RCV002450913
• dbSNP Id: rs748849177
• ExAC: 20:10620506 C / T
• gnomAD v2: 20-10620506-C-T
• gnomAD v3: 20-10639858-C-T
• gnomAD v4: 20-10639858-C-T
• MyVariant Identifiers: chr20:g.10620506C>T (hg19) ; chr20:g.10639858C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.10639858C>T , CM000682.2:g.10639858C>T	GRCh38
NC_000020.10:g.10620506C>T , CM000682.1:g.10620506C>T	GRCh37
NC_000020.9:g.10568506C>T	NCBI36
NG_007496.1:g.39189G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254958.10:c.3297G>A MANE Select	ENSP00000254958.4:p.Pro1099=
ENST00000254958.9:c.3297G>A	ENSP00000254958.4:p.Pro1099=
ENST00000423891.6:n.3163G>A
NM_000214.2:c.3297G>A	NP_000205.1:p.Pro1099=
NM_000214.3:c.3297G>A MANE Select	NP_000205.1:p.Pro1099=