Canonical Allele Identifier: CA356737252
Gene: PHOX2B HGNC NCBI

Linked Data

gnomAD v4: 4-41746025-C-T
MyVariant Identifiers: chr4:g.41748042C>T (hg19) chr4:g.41746025C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.41746025C>T , CM000666.2:g.41746025C>T GRCh38
NC_000004.11:g.41748042C>T , CM000666.1:g.41748042C>T GRCh37
NC_000004.10:g.41442799C>T NCBI36
NG_008243.1:g.7946G>A , LRG_513:g.7946G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000226382.4:c.727G>A MANE Select ENSP00000226382.2:p.Ala243Thr
ENST00000226382.3:c.727G>A ENSP00000226382.2:p.Ala243Thr
NM_003924.3:c.727G>A , LRG_513t1:c.727G>A NP_003915.2:p.Ala243Thr
NM_003924.4:c.727G>A MANE Select NP_003915.2:p.Ala243Thr
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