Canonical Allele Identifier: CA355759907

Gene: P3H2

Linked Data

• gnomAD v4: 3-189995390-T-G
• MyVariant Identifiers: chr3:g.189713179T>G (hg19) ; chr3:g.189995390T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.189995390T>G , CM000665.2:g.189995390T>G	GRCh38
NC_000003.11:g.189713179T>G , CM000665.1:g.189713179T>G	GRCh37
NC_000003.10:g.191195873T>G	NCBI36
NG_031929.1:g.132048A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319332.10:c.533A>C MANE Select	ENSP00000316881.5:p.Asn178Thr
ENST00000319332.9:c.533A>C	ENSP00000316881.5:p.Asn178Thr
ENST00000426003.1:c.-11A>C	ENSP00000394326.1:n.-11A>C
ENST00000427335.6:c.-11A>C	ENSP00000408947.2:n.-11A>C
ENST00000444866.5:c.-11A>C	ENSP00000391374.1:n.-11A>C
NM_001134418.1:c.-11A>C	NP_001127890.1:n.-11A>C
NM_018192.3:c.533A>C	NP_060662.2:p.Asn178Thr
XM_011512955.1:c.-11A>C	XP_011511257.1:n.-11A>C
NM_018192.4:c.533A>C MANE Select	NP_060662.2:p.Asn178Thr
NM_001134418.2:c.-11A>C	NP_001127890.1:n.-11A>C