Canonical Allele Identifier: CA783222376
Gene: GPX4 HGNC NCBI

Linked Data

dbSNP Id: rs1174004273
gnomAD v4: 19-1103967-G-C
MyVariant Identifiers: chr19:g.1103966G>C (hg19) chr19:g.1103967G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1103967G>C , CM000681.2:g.1103967G>C GRCh38
NC_000019.9:g.1103966G>C , CM000681.1:g.1103966G>C GRCh37
NC_000019.8:g.1054966G>C NCBI36
NG_050621.1:g.5042G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000354171.12:c.-77G>C ENSP00000346103.7:n.-77G>C
ENST00000616066.4:c.-77G>C ENSP00000485000.1:n.-77G>C
NM_001039847.2:c.-77G>C NP_001034936.1:n.-77G>C
NM_002085.4:c.-77G>C NP_002076.2:n.-77G>C
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