Canonical Allele Identifier: CA2161153648
Gene: JAG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.105150747G= , CM000676.2:g.105150747G= GRCh38
NC_000014.8:g.105617084G= , CM000676.1:g.105617084G= GRCh37
NC_000014.7:g.104688129G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000331782.8:c.1459C= MANE Select ENSP00000328169.3:p.Pro487=
ENST00000331782.7:c.1459C= ENSP00000328169.3:p.Pro487=
ENST00000347004.2:c.1345C= ENSP00000328566.2:p.Pro449=
NM_002226.4:c.1459C= NP_002217.3:p.Pro487=
NM_145159.2:c.1345C= NP_660142.1:p.Pro449=
XM_011536736.1:c.1459C= XP_011535038.1:p.Pro487=
XR_001750303.2:n.1520C=
NM_002226.5:c.1459C= MANE Select NP_002217.3:p.Pro487=
NM_145159.3:c.1345C= NP_660142.1:p.Pro449=