Canonical Allele Identifier: CA89743577
Gene: P3H2 HGNC NCBI

Linked Data

dbSNP Id: rs370898423

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.189995554dup , CM000665.2:g.189995554dup GRCh38
NC_000003.11:g.189713343dup , CM000665.1:g.189713343dup GRCh37
NC_000003.10:g.191196037dup NCBI36
NG_031929.1:g.131885dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000319332.10:c.481-111dup MANE Select ENSP00000316881.5:n.481-111dup
ENST00000319332.9:c.481-111dup ENSP00000316881.5:n.481-111dup
ENST00000426003.1:c.-63-111dup ENSP00000394326.1:n.-63-111dup
ENST00000427335.6:c.-63-111dup ENSP00000408947.2:n.-63-111dup
ENST00000444866.5:c.-63-111dup ENSP00000391374.1:n.-63-111dup
NM_001134418.1:c.-63-111dup NP_001127890.1:n.-63-111dup
NM_018192.3:c.481-111dup NP_060662.2:n.481-111dup
XM_011512955.1:c.-63-111dup XP_011511257.1:n.-63-111dup
NM_018192.4:c.481-111dup MANE Select NP_060662.2:n.481-111dup
NM_001134418.2:c.-63-111dup NP_001127890.1:n.-63-111dup