Canonical Allele Identifier: CA439143162
Gene: PHOX2B HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.41748187G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.41746170G>A , CM000666.2:g.41746170G>A GRCh38
NC_000004.11:g.41748187G>A , CM000666.1:g.41748187G>A GRCh37
NC_000004.10:g.41442944G>A NCBI36
NG_008243.1:g.7801C>T , LRG_513:g.7801C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000226382.4:c.582C>T MANE Select ENSP00000226382.2:p.Ser194=
ENST00000226382.3:c.582C>T ENSP00000226382.2:p.Ser194=
ENST00000510424.2:n.403C>T
NM_003924.3:c.582C>T , LRG_513t1:c.582C>T NP_003915.2:p.Ser194=
NM_003924.4:c.582C>T MANE Select NP_003915.2:p.Ser194=
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