Canonical Allele Identifier: CA992487250
Gene: GPX4 HGNC NCBI

Linked Data

dbSNP Id: rs2079618366
gnomAD v3: 19-1103966-A-G
gnomAD v4: 19-1103966-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1103966A>G , CM000681.2:g.1103966A>G GRCh38
NC_000019.9:g.1103965A>G , CM000681.1:g.1103965A>G GRCh37
NC_000019.8:g.1054965A>G NCBI36
NG_050621.1:g.5041A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000354171.12:c.-78A>G ENSP00000346103.7:n.-78A>G
ENST00000616066.4:c.-78A>G ENSP00000485000.1:n.-78A>G
NM_001039847.2:c.-78A>G NP_001034936.1:n.-78A>G
NM_002085.4:c.-78A>G NP_002076.2:n.-78A>G