Canonical Allele Identifier: CA2588205734
Gene: GPX4 HGNC NCBI

Linked Data

gnomAD v4: 19-1103960-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1103960T>C , CM000681.2:g.1103960T>C GRCh38
NC_000019.9:g.1103959T>C , CM000681.1:g.1103959T>C GRCh37
NC_000019.8:g.1054959T>C NCBI36
NG_050621.1:g.5035T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000354171.12:c.-84T>C ENSP00000346103.7:n.-84T>C
ENST00000616066.4:c.-84T>C ENSP00000485000.1:n.-84T>C
NM_001039847.2:c.-84T>C NP_001034936.1:n.-84T>C
NM_002085.4:c.-84T>C NP_002076.2:n.-84T>C