Canonical Allele Identifier: CA437418292

Gene: P3H2

Linked Data

• MyVariant Identifiers: chr3:g.189713163T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.189995374T>C , CM000665.2:g.189995374T>C	GRCh38
NC_000003.11:g.189713163T>C , CM000665.1:g.189713163T>C	GRCh37
NC_000003.10:g.191195857T>C	NCBI36
NG_031929.1:g.132064A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319332.10:c.549A>G MANE Select	ENSP00000316881.5:p.Glu183=
ENST00000319332.9:c.549A>G	ENSP00000316881.5:p.Glu183=
ENST00000426003.1:c.6A>G	ENSP00000394326.1:p.Glu2=
ENST00000427335.6:c.6A>G	ENSP00000408947.2:p.Glu2=
ENST00000444866.5:c.6A>G	ENSP00000391374.1:p.Glu2=
NM_001134418.1:c.6A>G	NP_001127890.1:p.Glu2=
NM_018192.3:c.549A>G	NP_060662.2:p.Glu183=
XM_011512955.1:c.6A>G	XP_011511257.1:p.Glu2=
NM_018192.4:c.549A>G MANE Select	NP_060662.2:p.Glu183=
NM_001134418.2:c.6A>G	NP_001127890.1:p.Glu2=