Canonical Allele Identifier: CA381746495
Gene: PHOX2A HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.71954878G>C (hg19) chr11:g.72243834G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72243834G>C , CM000673.2:g.72243834G>C GRCh38
NC_000011.9:g.71954878G>C , CM000673.1:g.71954878G>C GRCh37
NC_000011.8:g.71632526G>C NCBI36
NG_008169.1:g.5343C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000298231.5:c.171C>G MANE Select ENSP00000298231.5:p.Cys57Trp
ENST00000544057.1:n.85+1746C>G
NM_005169.3:c.171C>G NP_005160.2:p.Cys57Trp
NM_005169.4:c.171C>G MANE Select NP_005160.2:p.Cys57Trp
Search 100 bp 5'
Search 100 bp 3'