Canonical Allele Identifier: CA409095477

Gene: JPH2

Linked Data

• MyVariant Identifiers: chr20:g.42815220C>A (hg19) ; chr20:g.44186580C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44186580C>A , CM000682.2:g.44186580C>A	GRCh38
NC_000020.10:g.42815220C>A , CM000682.1:g.42815220C>A	GRCh37
NC_000020.9:g.42248634C>A	NCBI36
NG_031867.1:g.5999G>T , LRG_394:g.5999G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000372980.4:c.126G>T MANE Select	ENSP00000362071.3:p.Trp42Cys
ENST00000342272.3:c.126G>T	ENSP00000344590.3:p.Trp42Cys
ENST00000372980.3:c.126G>T	ENSP00000362071.3:p.Trp42Cys
NM_020433.4:c.126G>T , LRG_394t1:c.126G>T	NP_065166.2:p.Trp42Cys
NM_175913.3:c.126G>T	NP_787109.2:p.Trp42Cys
XM_006723832.2:c.126G>T	XP_006723895.1:p.Trp42Cys
XM_006723833.2:c.126G>T	XP_006723896.1:p.Trp42Cys
XM_006723833.4:c.126G>T	XP_006723896.1:p.Trp42Cys
NM_020433.5:c.126G>T MANE Select	NP_065166.2:p.Trp42Cys
NM_175913.4:c.126G>T	NP_787109.2:p.Trp42Cys