Canonical Allele Identifier: CA381747049
Gene: PHOX2A HGNC NCBI

Linked Data

dbSNP Id: rs1176426459
gnomAD v4: 11-72243911-C-T
MyVariant Identifiers: chr11:g.71954955C>T (hg19) chr11:g.72243911C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72243911C>T , CM000673.2:g.72243911C>T GRCh38
NC_000011.9:g.71954955C>T , CM000673.1:g.71954955C>T GRCh37
NC_000011.8:g.71632603C>T NCBI36
NG_008169.1:g.5266G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000298231.5:c.94G>A MANE Select ENSP00000298231.5:p.Gly32Ser
ENST00000544057.1:n.85+1669G>A
NM_005169.3:c.94G>A NP_005160.2:p.Gly32Ser
NM_005169.4:c.94G>A MANE Select NP_005160.2:p.Gly32Ser
Search 100 bp 5'
Search 100 bp 3'