Canonical Allele Identifier: CA2365659747

Gene: JPH2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44186589A= , CM000682.2:g.44186589A=	GRCh38
NC_000020.10:g.42815229A= , CM000682.1:g.42815229A=	GRCh37
NC_000020.9:g.42248643A=	NCBI36
NG_031867.1:g.5990T= , LRG_394:g.5990T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000372980.4:c.117T= MANE Select	ENSP00000362071.3:p.Ser39=
ENST00000342272.3:c.117T=	ENSP00000344590.3:p.Ser39=
ENST00000372980.3:c.117T=	ENSP00000362071.3:p.Ser39=
NM_020433.4:c.117T= , LRG_394t1:c.117T=	NP_065166.2:p.Ser39=
NM_175913.3:c.117T=	NP_787109.2:p.Ser39=
XM_006723832.2:c.117T=	XP_006723895.1:p.Ser39=
XM_006723833.2:c.117T=	XP_006723896.1:p.Ser39=
XM_006723833.4:c.117T=	XP_006723896.1:p.Ser39=
NM_020433.5:c.117T= MANE Select	NP_065166.2:p.Ser39=
NM_175913.4:c.117T=	NP_787109.2:p.Ser39=