Canonical Allele Identifier: CA1981904732
Gene: PHOX2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72243725T= , CM000673.2:g.72243725T= GRCh38
NC_000011.9:g.71954769T= , CM000673.1:g.71954769T= GRCh37
NC_000011.8:g.71632417T= NCBI36
NG_008169.1:g.5452A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000298231.5:c.217+63A= MANE Select ENSP00000298231.5:n.217+63A=
ENST00000544057.1:n.85+1855A=
NM_005169.3:c.217+63A= NP_005160.2:n.217+63A=
NM_005169.4:c.217+63A= MANE Select NP_005160.2:n.217+63A=