Canonical Allele Identifier: CA129876039
Gene: GPX3 HGNC NCBI

Linked Data

dbSNP Id: rs572320481
gnomAD v3: 5-151020539-G-A
gnomAD v4: 5-151020539-G-A
MyVariant Identifiers: chr5:g.150400100G>A (hg19) chr5:g.151020539G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151020539G>A , CM000667.2:g.151020539G>A GRCh38
NC_000005.9:g.150400100G>A , CM000667.1:g.150400100G>A GRCh37
NC_000005.8:g.150380293G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000622181.4:c.-116G>A ENSP00000484258.1:n.-116G>A
NM_002084.3:c.-116G>A NP_002075.2:n.-116G>A
NM_001329790.1:c.-116G>A NP_001316719.1:n.-116G>A
NM_002084.4:c.-116G>A NP_002075.2:n.-116G>A
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