Canonical Allele Identifier: CA2317520895
Gene: GPX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1106790C= , CM000681.2:g.1106790C= GRCh38
NC_000019.9:g.1106789C= , CM000681.1:g.1106789C= GRCh37
NC_000019.8:g.1057789C= NCBI36
NG_050621.1:g.7865C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000354171.12:c.*218C= ENSP00000346103.7:n.*218C=
ENST00000592940.2:n.1183C=