Canonical Allele Identifier: CA488731423

Gene: JAG2

Linked Data

• MyVariant Identifiers: chr14:g.105617046T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.105150709T>A , CM000676.2:g.105150709T>A	GRCh38
NC_000014.8:g.105617046T>A , CM000676.1:g.105617046T>A	GRCh37
NC_000014.7:g.104688091T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000331782.8:c.1497A>T MANE Select	ENSP00000328169.3:p.Arg499=
ENST00000331782.7:c.1497A>T	ENSP00000328169.3:p.Arg499=
ENST00000347004.2:c.1383A>T	ENSP00000328566.2:p.Arg461=
NM_002226.4:c.1497A>T	NP_002217.3:p.Arg499=
NM_145159.2:c.1383A>T	NP_660142.1:p.Arg461=
XM_011536736.1:c.1497A>T	XP_011535038.1:p.Arg499=
XR_001750303.2:n.1558A>T
NM_002226.5:c.1497A>T MANE Select	NP_002217.3:p.Arg499=
NM_145159.3:c.1383A>T	NP_660142.1:p.Arg461=