Canonical Allele Identifier: CA439142761
Gene: PHOX2B HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.41748313C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.41746296C>T , CM000666.2:g.41746296C>T GRCh38
NC_000004.11:g.41748313C>T , CM000666.1:g.41748313C>T GRCh37
NC_000004.10:g.41443070C>T NCBI36
NG_008243.1:g.7675G>A , LRG_513:g.7675G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000226382.4:c.456G>A MANE Select ENSP00000226382.2:p.Lys152=
ENST00000226382.3:c.456G>A ENSP00000226382.2:p.Lys152=
ENST00000510424.2:n.277G>A
NM_003924.3:c.456G>A , LRG_513t1:c.456G>A NP_003915.2:p.Lys152=
NM_003924.4:c.456G>A MANE Select NP_003915.2:p.Lys152=
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