Canonical Allele Identifier: CA510739618
Gene: JPH2 HGNC NCBI

Linked Data

gnomAD v4: 20-44159953-G-T
MyVariant Identifiers: chr20:g.42788593G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44159953G>T , CM000682.2:g.44159953G>T GRCh38
NC_000020.10:g.42788593G>T , CM000682.1:g.42788593G>T GRCh37
NC_000020.9:g.42222007G>T NCBI36
NG_031867.1:g.32626C>A , LRG_394:g.32626C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372980.4:c.834C>A MANE Select ENSP00000362071.3:p.Pro278=
ENST00000372980.3:c.834C>A ENSP00000362071.3:p.Pro278=
NM_020433.4:c.834C>A , LRG_394t1:c.834C>A NP_065166.2:p.Pro278=
XM_006723832.2:c.834C>A XP_006723895.1:p.Pro278=
NM_020433.5:c.834C>A MANE Select NP_065166.2:p.Pro278=
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