Canonical Allele Identifier: CA631018519
Gene: GPX4 HGNC NCBI

Linked Data

dbSNP Id: rs1451134759
gnomAD v2: 19-1103945-G-A
gnomAD v3: 19-1103946-G-A
gnomAD v4: 19-1103946-G-A
MyVariant Identifiers: chr19:g.1103945G>A (hg19) chr19:g.1103946G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1103946G>A , CM000681.2:g.1103946G>A GRCh38
NC_000019.9:g.1103945G>A , CM000681.1:g.1103945G>A GRCh37
NC_000019.8:g.1054945G>A NCBI36
NG_050621.1:g.5021G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000354171.12:c.-98G>A ENSP00000346103.7:n.-98G>A
ENST00000616066.4:c.-98G>A ENSP00000485000.1:n.-98G>A
NM_001039847.2:c.-98G>A NP_001034936.1:n.-98G>A
NM_002085.4:c.-98G>A NP_002076.2:n.-98G>A
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