Canonical Allele Identifier: CA992487267
Gene: GPX4 HGNC NCBI

Linked Data

dbSNP Id: rs2079618764
gnomAD v3: 19-1103992-C-T
gnomAD v4: 19-1103992-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1103992C>T , CM000681.2:g.1103992C>T GRCh38
NC_000019.9:g.1103991C>T , CM000681.1:g.1103991C>T GRCh37
NC_000019.8:g.1054991C>T NCBI36
NG_050621.1:g.5067C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000706713.1:c.-52C>T ENSP00000516510.1:n.-52C>T
ENST00000354171.12:c.-52C>T ENSP00000346103.7:n.-52C>T
ENST00000616066.4:c.-52C>T ENSP00000485000.1:n.-52C>T
NM_001039847.2:c.-52C>T NP_001034936.1:n.-52C>T
NM_002085.4:c.-52C>T NP_002076.2:n.-52C>T