Canonical Allele Identifier: CA2365626488
Gene: JPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44118612G= , CM000682.2:g.44118612G= GRCh38
NC_000020.10:g.42747252G= , CM000682.1:g.42747252G= GRCh37
NC_000020.9:g.42180666G= NCBI36
NG_031867.1:g.73967C= , LRG_394:g.73967C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372980.4:c.1181C= MANE Select ENSP00000362071.3:p.Ala394=
ENST00000372980.3:c.1181C= ENSP00000362071.3:p.Ala394=
NM_020433.4:c.1181C= , LRG_394t1:c.1181C= NP_065166.2:p.Ala394=
XM_006723832.2:c.1181C= XP_006723895.1:p.Ala394=
NM_020433.5:c.1181C= MANE Select NP_065166.2:p.Ala394=