Canonical Allele Identifier: CA2735530005
Gene: GPX4 HGNC NCBI

Linked Data

dbSNP Id: rs2145163580

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1103935A>T , CM000681.2:g.1103935A>T GRCh38
NC_000019.9:g.1103934A>T , CM000681.1:g.1103934A>T GRCh37
NC_000019.8:g.1054934A>T NCBI36
NG_050621.1:g.5010A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000616066.4:c.-109A>T ENSP00000485000.1:n.-109A>T
NM_001039847.2:c.-109A>T NP_001034936.1:n.-109A>T
NM_002085.4:c.-109A>T NP_002076.2:n.-109A>T