Canonical Allele Identifier: CA355759813

Gene: P3H2

Linked Data

• MyVariant Identifiers: chr3:g.189713140T>A (hg19) ; chr3:g.189995351T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.189995351T>A , CM000665.2:g.189995351T>A	GRCh38
NC_000003.11:g.189713140T>A , CM000665.1:g.189713140T>A	GRCh37
NC_000003.10:g.191195834T>A	NCBI36
NG_031929.1:g.132087A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319332.10:c.572A>T MANE Select	ENSP00000316881.5:p.Tyr191Phe
ENST00000319332.9:c.572A>T	ENSP00000316881.5:p.Tyr191Phe
ENST00000426003.1:c.29A>T	ENSP00000394326.1:p.Tyr10Phe
ENST00000427335.6:c.29A>T	ENSP00000408947.2:p.Tyr10Phe
ENST00000444866.5:c.29A>T	ENSP00000391374.1:p.Tyr10Phe
NM_001134418.1:c.29A>T	NP_001127890.1:p.Tyr10Phe
NM_018192.3:c.572A>T	NP_060662.2:p.Tyr191Phe
XM_011512955.1:c.29A>T	XP_011511257.1:p.Tyr10Phe
NM_018192.4:c.572A>T MANE Select	NP_060662.2:p.Tyr191Phe
NM_001134418.2:c.29A>T	NP_001127890.1:p.Tyr10Phe