Canonical Allele Identifier: CA356737960

Gene: PHOX2B

Linked Data

• MyVariant Identifiers: chr4:g.41748198C>T (hg19) ; chr4:g.41746181C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.41746181C>T , CM000666.2:g.41746181C>T	GRCh38
NC_000004.11:g.41748198C>T , CM000666.1:g.41748198C>T	GRCh37
NC_000004.10:g.41442955C>T	NCBI36
NG_008243.1:g.7790G>A , LRG_513:g.7790G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226382.4:c.571G>A MANE Select	ENSP00000226382.2:p.Asp191Asn
ENST00000226382.3:c.571G>A	ENSP00000226382.2:p.Asp191Asn
ENST00000510424.2:n.392G>A
NM_003924.3:c.571G>A , LRG_513t1:c.571G>A	NP_003915.2:p.Asp191Asn
NM_003924.4:c.571G>A MANE Select	NP_003915.2:p.Asp191Asn