Canonical Allele Identifier: CA2838464613
Gene: JPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44118634A>T , CM000682.2:g.44118634A>T GRCh38
NC_000020.10:g.42747274A>T , CM000682.1:g.42747274A>T GRCh37
NC_000020.9:g.42180688A>T NCBI36
NG_031867.1:g.73945T>A , LRG_394:g.73945T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372980.4:c.1170-11T>A MANE Select ENSP00000362071.3:n.1170-11T>A
ENST00000372980.3:c.1170-11T>A ENSP00000362071.3:n.1170-11T>A
NM_020433.4:c.1170-11T>A , LRG_394t1:c.1170-11T>A NP_065166.2:n.1170-11T>A
XM_006723832.2:c.1170-11T>A XP_006723895.1:n.1170-11T>A
NM_020433.5:c.1170-11T>A MANE Select NP_065166.2:n.1170-11T>A