Canonical Allele Identifier: CA2614940096
Gene: PHOX2A HGNC NCBI

Linked Data

gnomAD v4: 11-72243737-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72243737C>T , CM000673.2:g.72243737C>T GRCh38
NC_000011.9:g.71954781C>T , CM000673.1:g.71954781C>T GRCh37
NC_000011.8:g.71632429C>T NCBI36
NG_008169.1:g.5440G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000298231.5:c.217+51G>A MANE Select ENSP00000298231.5:n.217+51G>A
ENST00000544057.1:n.85+1843G>A
NM_005169.3:c.217+51G>A NP_005160.2:n.217+51G>A
NM_005169.4:c.217+51G>A MANE Select NP_005160.2:n.217+51G>A
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