Canonical Allele Identifier: CA2573049304
Gene: PHOX2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.41745990T= , CM000666.2:g.41745990T= GRCh38
NC_000004.11:g.41748007T= , CM000666.1:g.41748007T= GRCh37
NC_000004.10:g.41442764T= NCBI36
NG_008243.1:g.7981A= , LRG_513:g.7981A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000226382.4:c.762A= MANE Select ENSP00000226382.2:p.Ala254=
ENST00000226382.3:c.762A= ENSP00000226382.2:p.Ala254=
NM_003924.3:c.762A= , LRG_513t1:c.762A= NP_003915.2:p.Ala254=
NM_003924.4:c.762A= MANE Select NP_003915.2:p.Ala254=