Canonical Allele Identifier: CA356738782
Gene: PHOX2B HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.41748315T>A (hg19) chr4:g.41746298T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.41746298T>A , CM000666.2:g.41746298T>A GRCh38
NC_000004.11:g.41748315T>A , CM000666.1:g.41748315T>A GRCh37
NC_000004.10:g.41443072T>A NCBI36
NG_008243.1:g.7673A>T , LRG_513:g.7673A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000226382.4:c.454A>T MANE Select ENSP00000226382.2:p.Lys152Ter
ENST00000226382.3:c.454A>T ENSP00000226382.2:p.Lys152Ter
ENST00000510424.2:n.275A>T
NM_003924.3:c.454A>T , LRG_513t1:c.454A>T NP_003915.2:p.Lys152Ter
NM_003924.4:c.454A>T MANE Select NP_003915.2:p.Lys152Ter
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