Canonical Allele Identifier: CA356737374
Gene: PHOX2B HGNC NCBI

Linked Data

gnomAD v4: 4-41746060-C-G
MyVariant Identifiers: chr4:g.41748077C>G (hg19) chr4:g.41746060C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.41746060C>G , CM000666.2:g.41746060C>G GRCh38
NC_000004.11:g.41748077C>G , CM000666.1:g.41748077C>G GRCh37
NC_000004.10:g.41442834C>G NCBI36
NG_008243.1:g.7911G>C , LRG_513:g.7911G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000226382.4:c.692G>C MANE Select ENSP00000226382.2:p.Gly231Ala
ENST00000226382.3:c.692G>C ENSP00000226382.2:p.Gly231Ala
ENST00000510424.2:n.513G>C
NM_003924.3:c.692G>C , LRG_513t1:c.692G>C NP_003915.2:p.Gly231Ala
NM_003924.4:c.692G>C MANE Select NP_003915.2:p.Gly231Ala
Search 100 bp 5'
Search 100 bp 3'