Canonical Allele Identifier: CA303992391
Gene: GPX4 HGNC NCBI

Linked Data

dbSNP Id: rs770446223
gnomAD v3: 19-1103939-G-A
gnomAD v4: 19-1103939-G-A
MyVariant Identifiers: chr19:g.1103938G>A (hg19) chr19:g.1103939G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1103939G>A , CM000681.2:g.1103939G>A GRCh38
NC_000019.9:g.1103938G>A , CM000681.1:g.1103938G>A GRCh37
NC_000019.8:g.1054938G>A NCBI36
NG_050621.1:g.5014G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000354171.12:c.-105G>A ENSP00000346103.7:n.-105G>A
ENST00000616066.4:c.-105G>A ENSP00000485000.1:n.-105G>A
NM_001039847.2:c.-105G>A NP_001034936.1:n.-105G>A
NM_002085.4:c.-105G>A NP_002076.2:n.-105G>A
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