Canonical Allele Identifier: CA439142981
Gene: PHOX2B HGNC NCBI

Linked Data

gnomAD v4: 4-41745972-A-C
MyVariant Identifiers: chr4:g.41747989A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.41745972A>C , CM000666.2:g.41745972A>C GRCh38
NC_000004.11:g.41747989A>C , CM000666.1:g.41747989A>C GRCh37
NC_000004.10:g.41442746A>C NCBI36
NG_008243.1:g.7999T>G , LRG_513:g.7999T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000226382.4:c.780T>G MANE Select ENSP00000226382.2:p.Ala260=
ENST00000226382.3:c.780T>G ENSP00000226382.2:p.Ala260=
NM_003924.3:c.780T>G , LRG_513t1:c.780T>G NP_003915.2:p.Ala260=
NM_003924.4:c.780T>G MANE Select NP_003915.2:p.Ala260=
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Search 100 bp 3'