Canonical Allele Identifier: CA563599559

Gene: GPX3

Linked Data

• dbSNP Id: rs1175734643
• gnomAD v2: 5-150400103-T-C
• gnomAD v3: 5-151020542-T-C
• gnomAD v4: 5-151020542-T-C
• MyVariant Identifiers: chr5:g.150400103T>C (hg19) ; chr5:g.151020542T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151020542T>C , CM000667.2:g.151020542T>C	GRCh38
NC_000005.9:g.150400103T>C , CM000667.1:g.150400103T>C	GRCh37
NC_000005.8:g.150380296T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622181.4:c.-113T>C	ENSP00000484258.1:n.-113T>C
NM_002084.3:c.-113T>C	NP_002075.2:n.-113T>C
NM_001329790.1:c.-113T>C	NP_001316719.1:n.-113T>C
NM_002084.4:c.-113T>C	NP_002075.2:n.-113T>C