Canonical Allele Identifier: CA992487223
Gene: GPX4 HGNC NCBI

Linked Data

dbSNP Id: rs2079617928
gnomAD v3: 19-1103928-C-T
gnomAD v4: 19-1103928-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1103928C>T , CM000681.2:g.1103928C>T GRCh38
NC_000019.9:g.1103927C>T , CM000681.1:g.1103927C>T GRCh37
NC_000019.8:g.1054927C>T NCBI36
NG_050621.1:g.5003C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000616066.4:c.-116C>T ENSP00000485000.1:n.-116C>T
NM_001039847.2:c.-116C>T NP_001034936.1:n.-116C>T
NM_002085.4:c.-116C>T NP_002076.2:n.-116C>T