Canonical Allele Identifier: CA2161153631
Gene: JAG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.105150717G= , CM000676.2:g.105150717G= GRCh38
NC_000014.8:g.105617054G= , CM000676.1:g.105617054G= GRCh37
NC_000014.7:g.104688099G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000331782.8:c.1489C= MANE Select ENSP00000328169.3:p.Leu497=
ENST00000331782.7:c.1489C= ENSP00000328169.3:p.Leu497=
ENST00000347004.2:c.1375C= ENSP00000328566.2:p.Leu459=
NM_002226.4:c.1489C= NP_002217.3:p.Leu497=
NM_145159.2:c.1375C= NP_660142.1:p.Leu459=
XM_011536736.1:c.1489C= XP_011535038.1:p.Leu497=
XR_001750303.2:n.1550C=
NM_002226.5:c.1489C= MANE Select NP_002217.3:p.Leu497=
NM_145159.3:c.1375C= NP_660142.1:p.Leu459=