Canonical Allele Identifier: CA2588205693
Gene: GPX4 HGNC NCBI

Linked Data

gnomAD v4: 19-1103932-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1103932C>G , CM000681.2:g.1103932C>G GRCh38
NC_000019.9:g.1103931C>G , CM000681.1:g.1103931C>G GRCh37
NC_000019.8:g.1054931C>G NCBI36
NG_050621.1:g.5007C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000616066.4:c.-112C>G ENSP00000485000.1:n.-112C>G
NM_001039847.2:c.-112C>G NP_001034936.1:n.-112C>G
NM_002085.4:c.-112C>G NP_002076.2:n.-112C>G
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