Canonical Allele Identifier: CA2580071014
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1749601
ClinVar RCV Id: RCV002359709

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.41746176del , CM000666.2:g.41746176del GRCh38
NC_000004.11:g.41748193del , CM000666.1:g.41748193del GRCh37
NC_000004.10:g.41442950del NCBI36
NG_008243.1:g.7796del , LRG_513:g.7796del

Transcript Alleles

HGVS Amino-acid Change
ENST00000226382.4:c.577del MANE Select ENSP00000226382.2:p.Asp193ThrfsTer?
ENST00000226382.3:c.577del ENSP00000226382.2:p.Asp193ThrfsTer?
ENST00000510424.2:n.398del
NM_003924.3:c.577del , LRG_513t1:c.577del NP_003915.2:p.Asp193ThrfsTer?
NM_003924.4:c.577del MANE Select NP_003915.2:p.Asp193ThrfsTer?