Canonical Allele Identifier: CA2161153627
Gene: JAG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.105150707T= , CM000676.2:g.105150707T= GRCh38
NC_000014.8:g.105617044T= , CM000676.1:g.105617044T= GRCh37
NC_000014.7:g.104688089T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000331782.8:c.1499A= MANE Select ENSP00000328169.3:p.Asp500=
ENST00000331782.7:c.1499A= ENSP00000328169.3:p.Asp500=
ENST00000347004.2:c.1385A= ENSP00000328566.2:p.Asp462=
NM_002226.4:c.1499A= NP_002217.3:p.Asp500=
NM_145159.2:c.1385A= NP_660142.1:p.Asp462=
XM_011536736.1:c.1499A= XP_011535038.1:p.Asp500=
XR_001750303.2:n.1560A=
NM_002226.5:c.1499A= MANE Select NP_002217.3:p.Asp500=
NM_145159.3:c.1385A= NP_660142.1:p.Asp462=