Canonical Allele Identifier: CA356737891
Gene: PHOX2B HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.41748186T>C (hg19) chr4:g.41746169T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.41746169T>C , CM000666.2:g.41746169T>C GRCh38
NC_000004.11:g.41748186T>C , CM000666.1:g.41748186T>C GRCh37
NC_000004.10:g.41442943T>C NCBI36
NG_008243.1:g.7802A>G , LRG_513:g.7802A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000226382.4:c.583A>G MANE Select ENSP00000226382.2:p.Thr195Ala
ENST00000226382.3:c.583A>G ENSP00000226382.2:p.Thr195Ala
ENST00000510424.2:n.404A>G
NM_003924.3:c.583A>G , LRG_513t1:c.583A>G NP_003915.2:p.Thr195Ala
NM_003924.4:c.583A>G MANE Select NP_003915.2:p.Thr195Ala
Search 100 bp 5'
Search 100 bp 3'