Canonical Allele Identifier: CA2365626491
Gene: JPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44118616G= , CM000682.2:g.44118616G= GRCh38
NC_000020.10:g.42747256G= , CM000682.1:g.42747256G= GRCh37
NC_000020.9:g.42180670G= NCBI36
NG_031867.1:g.73963C= , LRG_394:g.73963C=

Transcript Alleles

HGVS Amino-acid change
ENST00000372980.4:c.1177C= MANE Select ENSP00000362071.3:p.His393=
ENST00000372980.3:c.1177C= ENSP00000362071.3:p.His393=
NM_020433.4:c.1177C= , LRG_394t1:c.1177C= NP_065166.2:p.His393=
XM_006723832.2:c.1177C= XP_006723895.1:p.His393=
NM_020433.5:c.1177C= MANE Select NP_065166.2:p.His393=