Canonical Allele Identifier: CA356737078
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 2502689
ClinVar RCV Id: RCV003229362
MyVariant Identifiers: chr4:g.41747950C>T (hg19) chr4:g.41745933C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.41745933C>T , CM000666.2:g.41745933C>T GRCh38
NC_000004.11:g.41747950C>T , CM000666.1:g.41747950C>T GRCh37
NC_000004.10:g.41442707C>T NCBI36
NG_008243.1:g.8038G>A , LRG_513:g.8038G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000226382.4:c.819G>A MANE Select ENSP00000226382.2:p.Trp273Ter
ENST00000226382.3:c.819G>A ENSP00000226382.2:p.Trp273Ter
NM_003924.3:c.819G>A , LRG_513t1:c.819G>A NP_003915.2:p.Trp273Ter
NM_003924.4:c.819G>A MANE Select NP_003915.2:p.Trp273Ter
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