Canonical Allele Identifier: CA303992438
Gene: GPX4 HGNC NCBI

Linked Data

dbSNP Id: rs569335216
gnomAD v3: 19-1103988-G-C
gnomAD v4: 19-1103988-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1103988G>C , CM000681.2:g.1103988G>C GRCh38
NC_000019.9:g.1103987G>C , CM000681.1:g.1103987G>C GRCh37
NC_000019.8:g.1054987G>C NCBI36
NG_050621.1:g.5063G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000706713.1:c.-56G>C ENSP00000516510.1:n.-56G>C
ENST00000354171.12:c.-56G>C ENSP00000346103.7:n.-56G>C
ENST00000616066.4:c.-56G>C ENSP00000485000.1:n.-56G>C
NM_001039847.2:c.-56G>C NP_001034936.1:n.-56G>C
NM_002085.4:c.-56G>C NP_002076.2:n.-56G>C