Canonical Allele Identifier: CA783222388
Gene: GPX4 HGNC NCBI

Linked Data

dbSNP Id: rs1213100884
gnomAD v4: 19-1103984-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1103984A>G , CM000681.2:g.1103984A>G GRCh38
NC_000019.9:g.1103983A>G , CM000681.1:g.1103983A>G GRCh37
NC_000019.8:g.1054983A>G NCBI36
NG_050621.1:g.5059A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000706713.1:c.-60A>G ENSP00000516510.1:n.-60A>G
ENST00000354171.12:c.-60A>G ENSP00000346103.7:n.-60A>G
ENST00000616066.4:c.-60A>G ENSP00000485000.1:n.-60A>G
NM_001039847.2:c.-60A>G NP_001034936.1:n.-60A>G
NM_002085.4:c.-60A>G NP_002076.2:n.-60A>G