Canonical Allele Identifier: CA355759905

Gene: P3H2

Linked Data

• MyVariant Identifiers: chr3:g.189713178G>C (hg19) ; chr3:g.189995389G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.189995389G>C , CM000665.2:g.189995389G>C	GRCh38
NC_000003.11:g.189713178G>C , CM000665.1:g.189713178G>C	GRCh37
NC_000003.10:g.191195872G>C	NCBI36
NG_031929.1:g.132049C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319332.10:c.534C>G MANE Select	ENSP00000316881.5:p.Asn178Lys
ENST00000319332.9:c.534C>G	ENSP00000316881.5:p.Asn178Lys
ENST00000426003.1:c.-10C>G	ENSP00000394326.1:n.-10C>G
ENST00000427335.6:c.-10C>G	ENSP00000408947.2:n.-10C>G
ENST00000444866.5:c.-10C>G	ENSP00000391374.1:n.-10C>G
NM_001134418.1:c.-10C>G	NP_001127890.1:n.-10C>G
NM_018192.3:c.534C>G	NP_060662.2:p.Asn178Lys
XM_011512955.1:c.-10C>G	XP_011511257.1:n.-10C>G
NM_018192.4:c.534C>G MANE Select	NP_060662.2:p.Asn178Lys
NM_001134418.2:c.-10C>G	NP_001127890.1:n.-10C>G