Canonical Allele Identifier: CA381746538
Gene: PHOX2A HGNC NCBI

Linked Data

dbSNP Id: rs1226641955
gnomAD v3: 11-72243838-T-C
gnomAD v4: 11-72243838-T-C
MyVariant Identifiers: chr11:g.71954882T>C (hg19) chr11:g.72243838T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72243838T>C , CM000673.2:g.72243838T>C GRCh38
NC_000011.9:g.71954882T>C , CM000673.1:g.71954882T>C GRCh37
NC_000011.8:g.71632530T>C NCBI36
NG_008169.1:g.5339A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000298231.5:c.167A>G MANE Select ENSP00000298231.5:p.Asn56Ser
ENST00000544057.1:n.85+1742A>G
NM_005169.3:c.167A>G NP_005160.2:p.Asn56Ser
NM_005169.4:c.167A>G MANE Select NP_005160.2:p.Asn56Ser
Search 100 bp 5'
Search 100 bp 3'