Canonical Allele Identifier: CA2588207968
Gene: GPX4 HGNC NCBI

Linked Data

gnomAD v4: 19-1106789-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1106789T>C , CM000681.2:g.1106789T>C GRCh38
NC_000019.9:g.1106788T>C , CM000681.1:g.1106788T>C GRCh37
NC_000019.8:g.1057788T>C NCBI36
NG_050621.1:g.7864T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000354171.12:c.*217T>C ENSP00000346103.7:n.*217T>C
ENST00000592940.2:n.1182T>C
NM_001039847.2:c.*149T>C NP_001034936.1:n.*149T>C
NM_001039848.2:c.*217T>C NP_001034937.1:n.*217T>C
NM_002085.4:c.*217T>C NP_002076.2:n.*217T>C
NM_001039848.3:c.*217T>C NP_001034937.1:n.*217T>C
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