Canonical Allele Identifier: CA2576544956
Gene: GPX4 HGNC NCBI

Linked Data

gnomAD v4: 19-1103961-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1103961G>A , CM000681.2:g.1103961G>A GRCh38
NC_000019.9:g.1103960G>A , CM000681.1:g.1103960G>A GRCh37
NC_000019.8:g.1054960G>A NCBI36
NG_050621.1:g.5036G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000354171.12:c.-83G>A ENSP00000346103.7:n.-83G>A
ENST00000616066.4:c.-83G>A ENSP00000485000.1:n.-83G>A
NM_001039847.2:c.-83G>A NP_001034936.1:n.-83G>A
NM_002085.4:c.-83G>A NP_002076.2:n.-83G>A