Canonical Allele Identifier: CA2670427200
Gene: PHOX2B HGNC NCBI

Linked Data

gnomAD v4: 4-41746374-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.41746374T>A , CM000666.2:g.41746374T>A GRCh38
NC_000004.11:g.41748391T>A , CM000666.1:g.41748391T>A GRCh37
NC_000004.10:g.41443148T>A NCBI36
NG_008243.1:g.7597A>T , LRG_513:g.7597A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000226382.4:c.430-52A>T MANE Select ENSP00000226382.2:n.430-52A>T
ENST00000226382.3:c.430-52A>T ENSP00000226382.2:n.430-52A>T
ENST00000510424.2:n.251-52A>T
NM_003924.3:c.430-52A>T , LRG_513t1:c.430-52A>T NP_003915.2:n.430-52A>T
NM_003924.4:c.430-52A>T MANE Select NP_003915.2:n.430-52A>T
Search 100 bp 5'
Search 100 bp 3'