Canonical Allele Identifier: CA381746755
Gene: PHOX2A HGNC NCBI

Linked Data

gnomAD v4: 11-72243869-C-A
MyVariant Identifiers: chr11:g.71954913C>A (hg19) chr11:g.72243869C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72243869C>A , CM000673.2:g.72243869C>A GRCh38
NC_000011.9:g.71954913C>A , CM000673.1:g.71954913C>A GRCh37
NC_000011.8:g.71632561C>A NCBI36
NG_008169.1:g.5308G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000298231.5:c.136G>T MANE Select ENSP00000298231.5:p.Gly46Trp
ENST00000544057.1:n.85+1711G>T
NM_005169.3:c.136G>T NP_005160.2:p.Gly46Trp
NM_005169.4:c.136G>T MANE Select NP_005160.2:p.Gly46Trp
Search 100 bp 5'
Search 100 bp 3'