Canonical Allele Identifier: CA303992433
Gene: GPX4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1326145
ClinVar RCV Id: RCV001786206
dbSNP Id: rs8178966
gnomAD v2: 19-1103971-C-T
gnomAD v3: 19-1103972-C-T
gnomAD v4: 19-1103972-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1103972C>T , CM000681.2:g.1103972C>T GRCh38
NC_000019.9:g.1103971C>T , CM000681.1:g.1103971C>T GRCh37
NC_000019.8:g.1054971C>T NCBI36
NG_050621.1:g.5047C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000354171.12:c.-72C>T ENSP00000346103.7:n.-72C>T
ENST00000616066.4:c.-72C>T ENSP00000485000.1:n.-72C>T
NM_001039847.2:c.-72C>T NP_001034936.1:n.-72C>T
NM_002085.4:c.-72C>T NP_002076.2:n.-72C>T