Canonical Allele Identifier: CA1981904782
Gene: PHOX2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72243833C= , CM000673.2:g.72243833C= GRCh38
NC_000011.9:g.71954877C= , CM000673.1:g.71954877C= GRCh37
NC_000011.8:g.71632525C= NCBI36
NG_008169.1:g.5344G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000298231.5:c.172G= MANE Select ENSP00000298231.5:p.Ala58=
ENST00000544057.1:n.85+1747G=
NM_005169.3:c.172G= NP_005160.2:p.Ala58=
NM_005169.4:c.172G= MANE Select NP_005160.2:p.Ala58=