Canonical Allele Identifier: CA439142893
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1666761
ClinVar RCV Id: RCV002203541
dbSNP Id: rs1733869488
MyVariant Identifiers: chr4:g.41747920G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.41745903G>T , CM000666.2:g.41745903G>T GRCh38
NC_000004.11:g.41747920G>T , CM000666.1:g.41747920G>T GRCh37
NC_000004.10:g.41442677G>T NCBI36
NG_008243.1:g.8068C>A , LRG_513:g.8068C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000226382.4:c.849C>A MANE Select ENSP00000226382.2:p.Ile283=
ENST00000226382.3:c.849C>A ENSP00000226382.2:p.Ile283=
NM_003924.3:c.849C>A , LRG_513t1:c.849C>A NP_003915.2:p.Ile283=
NM_003924.4:c.849C>A MANE Select NP_003915.2:p.Ile283=
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Search 100 bp 3'