Canonical Allele Identifier: CA2573156870
Gene: JAG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1665794
ClinVar RCV Id: RCV002193898
dbSNP Id: rs766999933

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.10645274A>C , CM000682.2:g.10645274A>C GRCh38
NC_000020.10:g.10625922A>C , CM000682.1:g.10625922A>C GRCh37
NC_000020.9:g.10573922A>C NCBI36
NG_007496.1:g.33773T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000254958.10:c.2114-18T>G MANE Select ENSP00000254958.4:n.2114-18T>G
ENST00000617965.2:n.2703-18T>G
ENST00000254958.9:c.2114-18T>G ENSP00000254958.4:n.2114-18T>G
ENST00000423891.6:n.1980-18T>G
ENST00000488480.2:n.511-18T>G
NM_000214.2:c.2114-18T>G NP_000205.1:n.2114-18T>G
NM_000214.3:c.2114-18T>G MANE Select NP_000205.1:n.2114-18T>G