Canonical Allele Identifier: CA2502088873
Gene: GPX4 HGNC NCBI

Linked Data

gnomAD v4: 19-1106791-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1106791T>C , CM000681.2:g.1106791T>C GRCh38
NC_000019.9:g.1106790T>C , CM000681.1:g.1106790T>C GRCh37
NC_000019.8:g.1057790T>C NCBI36
NG_050621.1:g.7866T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000592940.2:n.1184T>C