Canonical Allele Identifier: CA303992430
Gene: GPX4 HGNC NCBI

Linked Data

dbSNP Id: rs8178966
gnomAD v2: 19-1103971-C-A
gnomAD v3: 19-1103972-C-A
gnomAD v4: 19-1103972-C-A
MyVariant Identifiers: chr19:g.1103971C>A (hg19) chr19:g.1103972C>A (hg38)
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Genomic Alleles

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

Transcript Alleles

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