Canonical Allele Identifier: CA2588205689
Gene: GPX4 HGNC NCBI

Linked Data

gnomAD v4: 19-1103930-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1103930G>T , CM000681.2:g.1103930G>T GRCh38
NC_000019.9:g.1103929G>T , CM000681.1:g.1103929G>T GRCh37
NC_000019.8:g.1054929G>T NCBI36
NG_050621.1:g.5005G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000616066.4:c.-114G>T ENSP00000485000.1:n.-114G>T
NM_001039847.2:c.-114G>T NP_001034936.1:n.-114G>T
NM_002085.4:c.-114G>T NP_002076.2:n.-114G>T