Canonical Allele Identifier: CA2317518924
Gene: GPX4 HGNC NCBI

Linked Data

dbSNP Id: rs1051095555

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1103927T>A , CM000681.2:g.1103927T>A GRCh38
NC_000019.9:g.1103926T>A , CM000681.1:g.1103926T>A GRCh37
NC_000019.8:g.1054926T>A NCBI36
NG_050621.1:g.5002T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000616066.4:c.-117T>A ENSP00000485000.1:n.-117T>A
NM_001039847.2:c.-117T>A NP_001034936.1:n.-117T>A
NM_002085.4:c.-117T>A NP_002076.2:n.-117T>A