Canonical Allele Identifier: CA783222383
Gene: GPX4 HGNC NCBI

Linked Data

dbSNP Id: rs8178966
gnomAD v3: 19-1103972-C-G
gnomAD v4: 19-1103972-C-G

Genomic Alleles

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

Transcript Alleles

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