Canonical Allele Identifier: CA356737101

Gene: PHOX2B

Linked Data

• ClinVar Variation Id: 648649
• ClinVar RCV Id: RCV002234956 ; RCV003133636
• dbSNP Id: rs1577558821
• gnomAD v4: 4-41745943-C-A
• MyVariant Identifiers: chr4:g.41747960C>A (hg19) ; chr4:g.41745943C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.41745943C>A , CM000666.2:g.41745943C>A	GRCh38
NC_000004.11:g.41747960C>A , CM000666.1:g.41747960C>A	GRCh37
NC_000004.10:g.41442717C>A	NCBI36
NG_008243.1:g.8028G>T , LRG_513:g.8028G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226382.4:c.809G>T MANE Select	ENSP00000226382.2:p.Gly270Val
ENST00000226382.3:c.809G>T	ENSP00000226382.2:p.Gly270Val
NM_003924.3:c.809G>T , LRG_513t1:c.809G>T	NP_003915.2:p.Gly270Val
NM_003924.4:c.809G>T MANE Select	NP_003915.2:p.Gly270Val