Canonical Allele Identifier: CA2670427215
Gene: PHOX2B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.41746395del , CM000666.2:g.41746395del GRCh38
NC_000004.11:g.41748412del , CM000666.1:g.41748412del GRCh37
NC_000004.10:g.41443169del NCBI36
NG_008243.1:g.7576del , LRG_513:g.7576del

Transcript Alleles

HGVS Amino-acid Change
ENST00000226382.4:c.430-73del MANE Select ENSP00000226382.2:n.430-73del
ENST00000226382.3:c.430-73del ENSP00000226382.2:n.430-73del
ENST00000510424.2:n.251-73del
NM_003924.3:c.430-73del , LRG_513t1:c.430-73del NP_003915.2:n.430-73del
NM_003924.4:c.430-73del MANE Select NP_003915.2:n.430-73del