Canonical Allele Identifier: CA439143176

Gene: PHOX2B

Linked Data

• MyVariant Identifiers: chr4:g.41748193C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.41746176C>G , CM000666.2:g.41746176C>G	GRCh38
NC_000004.11:g.41748193C>G , CM000666.1:g.41748193C>G	GRCh37
NC_000004.10:g.41442950C>G	NCBI36
NG_008243.1:g.7795G>C , LRG_513:g.7795G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226382.4:c.576G>C MANE Select	ENSP00000226382.2:p.Pro192=
ENST00000226382.3:c.576G>C	ENSP00000226382.2:p.Pro192=
ENST00000510424.2:n.397G>C
NM_003924.3:c.576G>C , LRG_513t1:c.576G>C	NP_003915.2:p.Pro192=
NM_003924.4:c.576G>C MANE Select	NP_003915.2:p.Pro192=