Canonical Allele Identifier: CA1981904785
Gene: PHOX2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72243839T= , CM000673.2:g.72243839T= GRCh38
NC_000011.9:g.71954883T= , CM000673.1:g.71954883T= GRCh37
NC_000011.8:g.71632531T= NCBI36
NG_008169.1:g.5338A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000298231.5:c.166A= MANE Select ENSP00000298231.5:p.Asn56=
ENST00000544057.1:n.85+1741A=
NM_005169.3:c.166A= NP_005160.2:p.Asn56=
NM_005169.4:c.166A= MANE Select NP_005160.2:p.Asn56=