Canonical Allele Identifier: CA408061158
Gene: AVP HGNC NCBI

Linked Data

dbSNP Id: rs1428916029
gnomAD v4: 20-3082657-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3082657G>T , CM000682.2:g.3082657G>T GRCh38
NC_000020.10:g.3063303G>T , CM000682.1:g.3063303G>T GRCh37
NC_000020.9:g.3011303G>T NCBI36
NG_008663.1:g.7068C>A , LRG_715:g.7068C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.468C>A MANE Select ENSP00000369647.3:p.Phe156Leu
NM_000490.4:c.468C>A , LRG_715t1:c.468C>A NP_000481.2:p.Phe156Leu
XM_011529267.1:c.468C>A XP_011527569.1:p.Phe156Leu
XM_011529267.2:c.468C>A XP_011527569.1:p.Phe156Leu
NM_000490.5:c.468C>A MANE Select NP_000481.2:p.Phe156Leu