Canonical Allele Identifier: CA805660946

Gene: GPX3

Linked Data

• dbSNP Id: rs1198550051
• gnomAD v3: 5-151020446-G-A
• gnomAD v4: 5-151020446-G-A
• MyVariant Identifiers: chr5:g.150400007G>A (hg19) ; chr5:g.151020446G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151020446G>A , CM000667.2:g.151020446G>A	GRCh38
NC_000005.9:g.150400007G>A , CM000667.1:g.150400007G>A	GRCh37
NC_000005.8:g.150380200G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622181.4:c.-209G>A	ENSP00000484258.1:n.-209G>A
NM_002084.3:c.-209G>A	NP_002075.2:n.-209G>A
XR_944410.1:n.38C>T
NM_001329790.1:c.-209G>A	NP_001316719.1:n.-209G>A
NM_002084.4:c.-209G>A	NP_002075.2:n.-209G>A