Canonical Allele Identifier: CA2161153593
Gene: JAG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.105150646G= , CM000676.2:g.105150646G= GRCh38
NC_000014.8:g.105616983G= , CM000676.1:g.105616983G= GRCh37
NC_000014.7:g.104688028G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000331782.8:c.1560C= MANE Select ENSP00000328169.3:p.Phe520=
ENST00000331782.7:c.1560C= ENSP00000328169.3:p.Phe520=
ENST00000347004.2:c.1446C= ENSP00000328566.2:p.Phe482=
NM_002226.4:c.1560C= NP_002217.3:p.Phe520=
NM_145159.2:c.1446C= NP_660142.1:p.Phe482=
XM_011536736.1:c.1560C= XP_011535038.1:p.Phe520=
XR_001750303.2:n.1621C=
NM_002226.5:c.1560C= MANE Select NP_002217.3:p.Phe520=
NM_145159.3:c.1446C= NP_660142.1:p.Phe482=