Canonical Allele Identifier: CA1981904821
Gene: PHOX2A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72243929C= , CM000673.2:g.72243929C= GRCh38
NC_000011.9:g.71954973C= , CM000673.1:g.71954973C= GRCh37
NC_000011.8:g.71632621C= NCBI36
NG_008169.1:g.5248G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000298231.5:c.76G= MANE Select ENSP00000298231.5:p.Ala26=
ENST00000544057.1:n.85+1651G=
NM_005169.3:c.76G= NP_005160.2:p.Ala26=
NM_005169.4:c.76G= MANE Select NP_005160.2:p.Ala26=
Search 100 bp 5'
Search 100 bp 3'