Canonical Allele Identifier: CA2346405500
Gene: AVP HGNC NCBI

Linked Data

dbSNP Id: rs1319811973
gnomAD v3: 20-3082950-A-G
gnomAD v4: 20-3082950-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3082950A>G , CM000682.2:g.3082950A>G GRCh38
NC_000020.10:g.3063596A>G , CM000682.1:g.3063596A>G GRCh37
NC_000020.9:g.3011596A>G NCBI36
NG_008663.1:g.6775T>C , LRG_715:g.6775T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.322+27T>C MANE Select ENSP00000369647.3:n.322+27T>C
NM_000490.4:c.322+27T>C , LRG_715t1:c.322+27T>C NP_000481.2:n.322+27T>C
XM_011529267.1:c.322+27T>C XP_011527569.1:n.322+27T>C
XM_011529267.2:c.322+27T>C XP_011527569.1:n.322+27T>C
NM_000490.5:c.322+27T>C MANE Select NP_000481.2:n.322+27T>C