Canonical Allele Identifier: CA2588205696
Gene: GPX4 HGNC NCBI

Linked Data

gnomAD v4: 19-1103935-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1103935A>G , CM000681.2:g.1103935A>G GRCh38
NC_000019.9:g.1103934A>G , CM000681.1:g.1103934A>G GRCh37
NC_000019.8:g.1054934A>G NCBI36
NG_050621.1:g.5010A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000616066.4:c.-109A>G ENSP00000485000.1:n.-109A>G
NM_001039847.2:c.-109A>G NP_001034936.1:n.-109A>G
NM_002085.4:c.-109A>G NP_002076.2:n.-109A>G