Canonical Allele Identifier: CA408061593
Gene: AVP HGNC NCBI

Linked Data

ClinVar Variation Id: 1285212
ClinVar RCV Id: RCV001702024
dbSNP Id: rs121964890
gnomAD v4: 20-3083039-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3083039G>T , CM000682.2:g.3083039G>T GRCh38
NC_000020.10:g.3063685G>T , CM000682.1:g.3063685G>T GRCh37
NC_000020.9:g.3011685G>T NCBI36
NG_008663.1:g.6686C>A , LRG_715:g.6686C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000380293.3:c.260C>A MANE Select ENSP00000369647.3:p.Ser87Tyr
NM_000490.4:c.260C>A , LRG_715t1:c.260C>A NP_000481.2:p.Ser87Tyr
XM_011529267.1:c.260C>A XP_011527569.1:p.Ser87Tyr
XM_011529267.2:c.260C>A XP_011527569.1:p.Ser87Tyr
NM_000490.5:c.260C>A MANE Select NP_000481.2:p.Ser87Tyr