Canonical Allele Identifier: CA2317518927
Gene: GPX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1103941G= , CM000681.2:g.1103941G= GRCh38
NC_000019.9:g.1103940G= , CM000681.1:g.1103940G= GRCh37
NC_000019.8:g.1054940G= NCBI36
NG_050621.1:g.5016G=

Transcript Alleles

HGVS Amino-acid change
ENST00000354171.12:c.-103G= ENSP00000346103.7:n.-103G=
ENST00000616066.4:c.-103G= ENSP00000485000.1:n.-103G=
NM_001039847.2:c.-103G= NP_001034936.1:n.-103G=
NM_002085.4:c.-103G= NP_002076.2:n.-103G=