Canonical Allele Identifier: CA2317518922
Gene: GPX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1103926G= , CM000681.2:g.1103926G= GRCh38
NC_000019.9:g.1103925G= , CM000681.1:g.1103925G= GRCh37
NC_000019.8:g.1054925G= NCBI36
NG_050621.1:g.5001G=

Transcript Alleles

HGVS Amino-acid change
ENST00000616066.4:c.-118G= ENSP00000485000.1:n.-118G=
NM_001039847.2:c.-118G= NP_001034936.1:n.-118G=
NM_002085.4:c.-118G= NP_002076.2:n.-118G=