Canonical Allele Identifier: CA783222380
Gene: GPX4 HGNC NCBI

Linked Data

dbSNP Id: rs1194859941

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1103969A>T , CM000681.2:g.1103969A>T GRCh38
NC_000019.9:g.1103968A>T , CM000681.1:g.1103968A>T GRCh37
NC_000019.8:g.1054968A>T NCBI36
NG_050621.1:g.5044A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000354171.12:c.-75A>T ENSP00000346103.7:n.-75A>T
ENST00000616066.4:c.-75A>T ENSP00000485000.1:n.-75A>T
NM_001039847.2:c.-75A>T NP_001034936.1:n.-75A>T
NM_002085.4:c.-75A>T NP_002076.2:n.-75A>T