Canonical Allele Identifier: CA2901414
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 858862
ClinVar RCV Id: RCV001064838 RCV002418533
dbSNP Id: rs765369462
ExAC: 4:41747966 C / T
gnomAD v2: 4-41747966-C-T
gnomAD v4: 4-41745949-C-T
MyVariant Identifiers: chr4:g.41747966C>T (hg19) chr4:g.41745949C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.41745949C>T , CM000666.2:g.41745949C>T GRCh38
NC_000004.11:g.41747966C>T , CM000666.1:g.41747966C>T GRCh37
NC_000004.10:g.41442723C>T NCBI36
NG_008243.1:g.8022G>A , LRG_513:g.8022G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000226382.4:c.803G>A MANE Select ENSP00000226382.2:p.Gly268Asp
ENST00000226382.3:c.803G>A ENSP00000226382.2:p.Gly268Asp
NM_003924.3:c.803G>A , LRG_513t1:c.803G>A NP_003915.2:p.Gly268Asp
NM_003924.4:c.803G>A MANE Select NP_003915.2:p.Gly268Asp
Search 100 bp 5'
Search 100 bp 3'