Canonical Allele Identifier: CA2839666912
Gene: JPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44118480C>A , CM000682.2:g.44118480C>A GRCh38
NC_000020.10:g.42747120C>A , CM000682.1:g.42747120C>A GRCh37
NC_000020.9:g.42180534C>A NCBI36
NG_031867.1:g.74099G>T , LRG_394:g.74099G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372980.4:c.1288+25G>T MANE Select ENSP00000362071.3:n.1288+25G>T
ENST00000372980.3:c.1288+25G>T ENSP00000362071.3:n.1288+25G>T
NM_020433.4:c.1288+25G>T , LRG_394t1:c.1288+25G>T NP_065166.2:n.1288+25G>T
XM_006723832.2:c.1288+25G>T XP_006723895.1:n.1288+25G>T
NM_020433.5:c.1288+25G>T MANE Select NP_065166.2:n.1288+25G>T