Canonical Allele Identifier: CA408061377
Gene: AVP HGNC NCBI

Linked Data

gnomAD v4: 20-3082767-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3082767A>G , CM000682.2:g.3082767A>G GRCh38
NC_000020.10:g.3063413A>G , CM000682.1:g.3063413A>G GRCh37
NC_000020.9:g.3011413A>G NCBI36
NG_008663.1:g.6958T>C , LRG_715:g.6958T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.358T>C MANE Select ENSP00000369647.3:p.Phe120Leu
NM_000490.4:c.358T>C , LRG_715t1:c.358T>C NP_000481.2:p.Phe120Leu
XM_011529267.1:c.358T>C XP_011527569.1:p.Phe120Leu
XM_011529267.2:c.358T>C XP_011527569.1:p.Phe120Leu
NM_000490.5:c.358T>C MANE Select NP_000481.2:p.Phe120Leu