Canonical Allele Identifier: CA2161153671
Gene: JAG2 HGNC NCBI
MIR6765 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.105150802T= , CM000676.2:g.105150802T= GRCh38
NC_000014.8:g.105617139T= , CM000676.1:g.105617139T= GRCh37
NC_000014.7:g.104688184T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000331782.8:c.1429-25A= (JAG2) MANE Select ENSP00000328169.3:n.1429-25A=
ENST00000331782.7:c.1429-25A= (JAG2) ENSP00000328169.3:n.1429-25A=
ENST00000347004.2:c.1315-25A= (JAG2) ENSP00000328566.2:n.1315-25A=
NM_002226.4:c.1429-25A= (JAG2) NP_002217.3:n.1429-25A=
NM_145159.2:c.1315-25A= (JAG2) NP_660142.1:n.1315-25A=
NR_106823.1:n.63A= (MIR6765)
XM_011536736.1:c.1429-25A= (JAG2) XP_011535038.1:n.1429-25A=
XR_001750303.2:n.1490-25A= (JAG2)
NM_002226.5:c.1429-25A= (JAG2) MANE Select NP_002217.3:n.1429-25A=
NM_145159.3:c.1315-25A= (JAG2) NP_660142.1:n.1315-25A=
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