Canonical Allele Identifier: CA303992395
Gene: GPX4 HGNC NCBI

Linked Data

dbSNP Id: rs548265258
gnomAD v2: 19-1103940-G-T
gnomAD v3: 19-1103941-G-T
gnomAD v4: 19-1103941-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1103941G>T , CM000681.2:g.1103941G>T GRCh38
NC_000019.9:g.1103940G>T , CM000681.1:g.1103940G>T GRCh37
NC_000019.8:g.1054940G>T NCBI36
NG_050621.1:g.5016G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000354171.12:c.-103G>T ENSP00000346103.7:n.-103G>T
ENST00000616066.4:c.-103G>T ENSP00000485000.1:n.-103G>T
NM_001039847.2:c.-103G>T NP_001034936.1:n.-103G>T
NM_002085.4:c.-103G>T NP_002076.2:n.-103G>T