Canonical Allele Identifier: CA2588205759
Gene: GPX4 HGNC NCBI

Linked Data

gnomAD v4: 19-1103985-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1103985C>T , CM000681.2:g.1103985C>T GRCh38
NC_000019.9:g.1103984C>T , CM000681.1:g.1103984C>T GRCh37
NC_000019.8:g.1054984C>T NCBI36
NG_050621.1:g.5060C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000706713.1:c.-59C>T ENSP00000516510.1:n.-59C>T
ENST00000354171.12:c.-59C>T ENSP00000346103.7:n.-59C>T
ENST00000616066.4:c.-59C>T ENSP00000485000.1:n.-59C>T
NM_001039847.2:c.-59C>T NP_001034936.1:n.-59C>T
NM_002085.4:c.-59C>T NP_002076.2:n.-59C>T
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