Canonical Allele Identifier: CA356738055
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 970401
ClinVar RCV Id: RCV001245967
dbSNP Id: rs1191400815
MyVariant Identifiers: chr4:g.41748209G>A (hg19) chr4:g.41746192G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.41746192G>A , CM000666.2:g.41746192G>A GRCh38
NC_000004.11:g.41748209G>A , CM000666.1:g.41748209G>A GRCh37
NC_000004.10:g.41442966G>A NCBI36
NG_008243.1:g.7779C>T , LRG_513:g.7779C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000226382.4:c.560C>T MANE Select ENSP00000226382.2:p.Ala187Val
ENST00000226382.3:c.560C>T ENSP00000226382.2:p.Ala187Val
ENST00000510424.2:n.381C>T
NM_003924.3:c.560C>T , LRG_513t1:c.560C>T NP_003915.2:p.Ala187Val
NM_003924.4:c.560C>T MANE Select NP_003915.2:p.Ala187Val
Search 100 bp 5'
Search 100 bp 3'