Canonical Allele Identifier: CA2676033022
Gene: GPX3 HGNC NCBI

Linked Data

gnomAD v4: 5-151020435-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151020435A>G , CM000667.2:g.151020435A>G GRCh38
NC_000005.9:g.150399996A>G , CM000667.1:g.150399996A>G GRCh37
NC_000005.8:g.150380189A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_944410.1:n.49T>C
NM_001329790.1:c.-220A>G NP_001316719.1:n.-220A>G
NM_002084.4:c.-220A>G NP_002075.2:n.-220A>G
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