Canonical Allele Identifier: CA2676033032
Gene: GPX3 HGNC NCBI

Linked Data

gnomAD v4: 5-151020448-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151020448G>T , CM000667.2:g.151020448G>T GRCh38
NC_000005.9:g.150400009G>T , CM000667.1:g.150400009G>T GRCh37
NC_000005.8:g.150380202G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000622181.4:c.-207G>T ENSP00000484258.1:n.-207G>T
NM_002084.3:c.-207G>T NP_002075.2:n.-207G>T
XR_944410.1:n.36C>A
NM_001329790.1:c.-207G>T NP_001316719.1:n.-207G>T
NM_002084.4:c.-207G>T NP_002075.2:n.-207G>T
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