Canonical Allele Identifier: CA2588205754
Gene: GPX4 HGNC NCBI

Linked Data

gnomAD v4: 19-1103981-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1103981C>A , CM000681.2:g.1103981C>A GRCh38
NC_000019.9:g.1103980C>A , CM000681.1:g.1103980C>A GRCh37
NC_000019.8:g.1054980C>A NCBI36
NG_050621.1:g.5056C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000354171.12:c.-63C>A ENSP00000346103.7:n.-63C>A
ENST00000616066.4:c.-63C>A ENSP00000485000.1:n.-63C>A
NM_001039847.2:c.-63C>A NP_001034936.1:n.-63C>A
NM_002085.4:c.-63C>A NP_002076.2:n.-63C>A