Canonical Allele Identifier: CA2161153655
Gene: JAG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.105150764C= , CM000676.2:g.105150764C= GRCh38
NC_000014.8:g.105617101C= , CM000676.1:g.105617101C= GRCh37
NC_000014.7:g.104688146C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000331782.8:c.1442G= MANE Select ENSP00000328169.3:p.Gly481=
ENST00000331782.7:c.1442G= ENSP00000328169.3:p.Gly481=
ENST00000347004.2:c.1328G= ENSP00000328566.2:p.Gly443=
NM_002226.4:c.1442G= NP_002217.3:p.Gly481=
NM_145159.2:c.1328G= NP_660142.1:p.Gly443=
XM_011536736.1:c.1442G= XP_011535038.1:p.Gly481=
XR_001750303.2:n.1503G=
NM_002226.5:c.1442G= MANE Select NP_002217.3:p.Gly481=
NM_145159.3:c.1328G= NP_660142.1:p.Gly443=