Canonical Allele Identifier: CA2317518932
Gene: GPX4 HGNC NCBI

Linked Data

dbSNP Id: rs2079618064
gnomAD v4: 19-1103945-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1103945T>C , CM000681.2:g.1103945T>C GRCh38
NC_000019.9:g.1103944T>C , CM000681.1:g.1103944T>C GRCh37
NC_000019.8:g.1054944T>C NCBI36
NG_050621.1:g.5020T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000354171.12:c.-99T>C ENSP00000346103.7:n.-99T>C
ENST00000616066.4:c.-99T>C ENSP00000485000.1:n.-99T>C
NM_001039847.2:c.-99T>C NP_001034936.1:n.-99T>C
NM_002085.4:c.-99T>C NP_002076.2:n.-99T>C
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