Canonical Allele Identifier: CA2586973800
Gene: PHOX2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.41746047_41746095del , CM000666.2:g.41746047_41746095del GRCh38
NC_000004.11:g.41748064_41748112del , CM000666.1:g.41748064_41748112del GRCh37
NC_000004.10:g.41442821_41442869del NCBI36
NG_008243.1:g.7882_7930del , LRG_513:g.7882_7930del

Transcript Alleles

HGVS Amino-acid Change
ENST00000226382.4:c.663_711del MANE Select ENSP00000226382.2:p.Gly222ArgfsTer?
ENST00000226382.3:c.663_711del ENSP00000226382.2:p.Gly222ArgfsTer?
ENST00000510424.2:n.484_532del
NM_003924.3:c.663_711del , LRG_513t1:c.663_711del NP_003915.2:p.Gly222ArgfsTer?
NM_003924.4:c.663_711del MANE Select NP_003915.2:p.Gly222ArgfsTer?