Canonical Allele Identifier: CA2317518956
Gene: GPX4 HGNC NCBI

Linked Data

dbSNP Id: rs1174004273
gnomAD v4: 19-1103967-G-A

Genomic Alleles

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

Transcript Alleles

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