Canonical Allele Identifier: CA2792651241
Gene: PHOX2A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72243722A>G , CM000673.2:g.72243722A>G GRCh38
NC_000011.9:g.71954766A>G , CM000673.1:g.71954766A>G GRCh37
NC_000011.8:g.71632414A>G NCBI36
NG_008169.1:g.5455T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000298231.5:c.217+66T>C MANE Select ENSP00000298231.5:n.217+66T>C
ENST00000544057.1:n.85+1858T>C
NM_005169.3:c.217+66T>C NP_005160.2:n.217+66T>C
NM_005169.4:c.217+66T>C MANE Select NP_005160.2:n.217+66T>C
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