Canonical Allele Identifier: CA2670427199
Gene: PHOX2B HGNC NCBI

Linked Data

dbSNP Id: rs1733901212
gnomAD v4: 4-41746374-T-C

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000226382.4:c.430-52A>G MANE Select ENSP00000226382.2:n.430-52A>G
ENST00000226382.3:c.430-52A>G ENSP00000226382.2:n.430-52A>G
ENST00000510424.2:n.251-52A>G
NM_003924.3:c.430-52A>G , LRG_513t1:c.430-52A>G NP_003915.2:n.430-52A>G
NM_003924.4:c.430-52A>G MANE Select NP_003915.2:n.430-52A>G