Canonical Allele Identifier: CA2365647683
Gene: JPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44160034G= , CM000682.2:g.44160034G= GRCh38
NC_000020.10:g.42788674G= , CM000682.1:g.42788674G= GRCh37
NC_000020.9:g.42222088G= NCBI36
NG_031867.1:g.32545C= , LRG_394:g.32545C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372980.4:c.753C= MANE Select ENSP00000362071.3:p.Ser251=
ENST00000372980.3:c.753C= ENSP00000362071.3:p.Ser251=
NM_020433.4:c.753C= , LRG_394t1:c.753C= NP_065166.2:p.Ser251=
XM_006723832.2:c.753C= XP_006723895.1:p.Ser251=
NM_020433.5:c.753C= MANE Select NP_065166.2:p.Ser251=