Canonical Allele Identifier: CA408061164
Gene: AVP HGNC NCBI

Linked Data

gnomAD v4: 20-3082659-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3082659A>T , CM000682.2:g.3082659A>T GRCh38
NC_000020.10:g.3063305A>T , CM000682.1:g.3063305A>T GRCh37
NC_000020.9:g.3011305A>T NCBI36
NG_008663.1:g.7066T>A , LRG_715:g.7066T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.466T>A MANE Select ENSP00000369647.3:p.Phe156Ile
NM_000490.4:c.466T>A , LRG_715t1:c.466T>A NP_000481.2:p.Phe156Ile
XM_011529267.1:c.466T>A XP_011527569.1:p.Phe156Ile
XM_011529267.2:c.466T>A XP_011527569.1:p.Phe156Ile
NM_000490.5:c.466T>A MANE Select NP_000481.2:p.Phe156Ile