Canonical Allele Identifier: CA2497074314
Gene: PHOX2B HGNC NCBI

Linked Data

dbSNP Id: rs1733900560

Genomic Alleles

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

Transcript Alleles

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