Canonical Allele Identifier: CA356737179
Gene: PHOX2B HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.41748006C>G (hg19) chr4:g.41745989C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.41745989C>G , CM000666.2:g.41745989C>G GRCh38
NC_000004.11:g.41748006C>G , CM000666.1:g.41748006C>G GRCh37
NC_000004.10:g.41442763C>G NCBI36
NG_008243.1:g.7982G>C , LRG_513:g.7982G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000226382.4:c.763G>C MANE Select ENSP00000226382.2:p.Ala255Pro
ENST00000226382.3:c.763G>C ENSP00000226382.2:p.Ala255Pro
NM_003924.3:c.763G>C , LRG_513t1:c.763G>C NP_003915.2:p.Ala255Pro
NM_003924.4:c.763G>C MANE Select NP_003915.2:p.Ala255Pro
Search 100 bp 5'
Search 100 bp 3'