Canonical Allele Identifier: CA2705770668
Gene: PHOX2B HGNC NCBI

Linked Data

dbSNP Id: rs2153112826

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.41746346del , CM000666.2:g.41746346del GRCh38
NC_000004.11:g.41748363del , CM000666.1:g.41748363del GRCh37
NC_000004.10:g.41443120del NCBI36
NG_008243.1:g.7625del , LRG_513:g.7625del

Transcript Alleles

HGVS Amino-acid Change
ENST00000226382.4:c.430-24del MANE Select ENSP00000226382.2:n.430-24del
ENST00000226382.3:c.430-24del ENSP00000226382.2:n.430-24del
ENST00000510424.2:n.251-24del
NM_003924.3:c.430-24del , LRG_513t1:c.430-24del NP_003915.2:n.430-24del
NM_003924.4:c.430-24del MANE Select NP_003915.2:n.430-24del