Canonical Allele Identifier: CA783222387
Gene: GPX4 HGNC NCBI

Linked Data

dbSNP Id: rs1280961351
gnomAD v4: 19-1103980-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1103980G>A , CM000681.2:g.1103980G>A GRCh38
NC_000019.9:g.1103979G>A , CM000681.1:g.1103979G>A GRCh37
NC_000019.8:g.1054979G>A NCBI36
NG_050621.1:g.5055G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000354171.12:c.-64G>A ENSP00000346103.7:n.-64G>A
ENST00000616066.4:c.-64G>A ENSP00000485000.1:n.-64G>A
NM_001039847.2:c.-64G>A NP_001034936.1:n.-64G>A
NM_002085.4:c.-64G>A NP_002076.2:n.-64G>A