Canonical Allele Identifier: CA2588205686
Gene: GPX4 HGNC NCBI

Linked Data

dbSNP Id: rs1051095555
gnomAD v4: 19-1103927-T-G

Genomic Alleles

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

Transcript Alleles

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