Canonical Allele Identifier: CA1981904738
Gene: PHOX2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72243734G= , CM000673.2:g.72243734G= GRCh38
NC_000011.9:g.71954778G= , CM000673.1:g.71954778G= GRCh37
NC_000011.8:g.71632426G= NCBI36
NG_008169.1:g.5443C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000298231.5:c.217+54C= MANE Select ENSP00000298231.5:n.217+54C=
ENST00000544057.1:n.85+1846C=
NM_005169.3:c.217+54C= NP_005160.2:n.217+54C=
NM_005169.4:c.217+54C= MANE Select NP_005160.2:n.217+54C=