Canonical Allele Identifier: CA634328989
Gene: AVP HGNC NCBI

Linked Data

dbSNP Id: rs1208534009
gnomAD v2: 20-3063589-C-A
gnomAD v3: 20-3082943-C-A
gnomAD v4: 20-3082943-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3082943C>A , CM000682.2:g.3082943C>A GRCh38
NC_000020.10:g.3063589C>A , CM000682.1:g.3063589C>A GRCh37
NC_000020.9:g.3011589C>A NCBI36
NG_008663.1:g.6782G>T , LRG_715:g.6782G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.322+34G>T MANE Select ENSP00000369647.3:n.322+34G>T
NM_000490.4:c.322+34G>T , LRG_715t1:c.322+34G>T NP_000481.2:n.322+34G>T
XM_011529267.1:c.322+34G>T XP_011527569.1:n.322+34G>T
XM_011529267.2:c.322+34G>T XP_011527569.1:n.322+34G>T
NM_000490.5:c.322+34G>T MANE Select NP_000481.2:n.322+34G>T