Canonical Allele Identifier: CA2588205729
Gene: GPX4 HGNC NCBI

Linked Data

gnomAD v4: 19-1103958-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1103958C>T , CM000681.2:g.1103958C>T GRCh38
NC_000019.9:g.1103957C>T , CM000681.1:g.1103957C>T GRCh37
NC_000019.8:g.1054957C>T NCBI36
NG_050621.1:g.5033C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000354171.12:c.-86C>T ENSP00000346103.7:n.-86C>T
ENST00000616066.4:c.-86C>T ENSP00000485000.1:n.-86C>T
NM_001039847.2:c.-86C>T NP_001034936.1:n.-86C>T
NM_002085.4:c.-86C>T NP_002076.2:n.-86C>T