Canonical Allele Identifier: CA2578074980
Gene: PHOX2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.41746360del , CM000666.2:g.41746360del GRCh38
NC_000004.11:g.41748377del , CM000666.1:g.41748377del GRCh37
NC_000004.10:g.41443134del NCBI36
NG_008243.1:g.7615del , LRG_513:g.7615del

Transcript Alleles

HGVS Amino-acid Change
ENST00000226382.4:c.430-34del MANE Select ENSP00000226382.2:n.430-34del
ENST00000226382.3:c.430-34del ENSP00000226382.2:n.430-34del
ENST00000510424.2:n.251-34del
NM_003924.3:c.430-34del , LRG_513t1:c.430-34del NP_003915.2:n.430-34del
NM_003924.4:c.430-34del MANE Select NP_003915.2:n.430-34del