Canonical Allele Identifier: CA355759940

Gene: P3H2

Linked Data

• MyVariant Identifiers: chr3:g.189713195T>C (hg19) ; chr3:g.189995406T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.189995406T>C , CM000665.2:g.189995406T>C	GRCh38
NC_000003.11:g.189713195T>C , CM000665.1:g.189713195T>C	GRCh37
NC_000003.10:g.191195889T>C	NCBI36
NG_031929.1:g.132032A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319332.10:c.517A>G MANE Select	ENSP00000316881.5:p.Thr173Ala
ENST00000319332.9:c.517A>G	ENSP00000316881.5:p.Thr173Ala
ENST00000426003.1:c.-27A>G	ENSP00000394326.1:n.-27A>G
ENST00000427335.6:c.-27A>G	ENSP00000408947.2:n.-27A>G
ENST00000444866.5:c.-27A>G	ENSP00000391374.1:n.-27A>G
NM_001134418.1:c.-27A>G	NP_001127890.1:n.-27A>G
NM_018192.3:c.517A>G	NP_060662.2:p.Thr173Ala
XM_011512955.1:c.-27A>G	XP_011511257.1:n.-27A>G
NM_018192.4:c.517A>G MANE Select	NP_060662.2:p.Thr173Ala
NM_001134418.2:c.-27A>G	NP_001127890.1:n.-27A>G