Canonical Allele Identifier: CA475598394
Gene: PHOX2A HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.71954992G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72243948G>C , CM000673.2:g.72243948G>C GRCh38
NC_000011.9:g.71954992G>C , CM000673.1:g.71954992G>C GRCh37
NC_000011.8:g.71632640G>C NCBI36
NG_008169.1:g.5229C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000298231.5:c.57C>G MANE Select ENSP00000298231.5:p.Ser19=
ENST00000544057.1:n.85+1632C>G
NM_005169.3:c.57C>G NP_005160.2:p.Ser19=
NM_005169.4:c.57C>G MANE Select NP_005160.2:p.Ser19=
Search 100 bp 5'
Search 100 bp 3'