Canonical Allele Identifier: CA2901406
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1079531
ClinVar RCV Id: RCV001394826 RCV002438902
dbSNP Id: rs761468808
ExAC: 4:41747935 G / A
gnomAD v2: 4-41747935-G-A
gnomAD v3: 4-41745918-G-A
gnomAD v4: 4-41745918-G-A
MyVariant Identifiers: chr4:g.41747935G>A (hg19) chr4:g.41745918G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.41745918G>A , CM000666.2:g.41745918G>A GRCh38
NC_000004.11:g.41747935G>A , CM000666.1:g.41747935G>A GRCh37
NC_000004.10:g.41442692G>A NCBI36
NG_008243.1:g.8053C>T , LRG_513:g.8053C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000226382.4:c.834C>T MANE Select ENSP00000226382.2:p.Gly278=
ENST00000226382.3:c.834C>T ENSP00000226382.2:p.Gly278=
NM_003924.3:c.834C>T , LRG_513t1:c.834C>T NP_003915.2:p.Gly278=
NM_003924.4:c.834C>T MANE Select NP_003915.2:p.Gly278=
Search 100 bp 5'
Search 100 bp 3'