Canonical Allele Identifier: CA310942881
Gene: AVP HGNC NCBI

Linked Data

ClinVar Variation Id: 2896713
ClinVar RCV Id: RCV003731069
dbSNP Id: rs566930108
gnomAD v2: 20-3063349-G-A
gnomAD v3: 20-3082703-G-A
gnomAD v4: 20-3082703-G-A
MyVariant Identifiers: chr20:g.3063349G>A (hg19) chr20:g.3063349_3063350delinsAC (hg19) chr20:g.3082703G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3082703G>A , CM000682.2:g.3082703G>A GRCh38
NC_000020.10:g.3063349G>A , CM000682.1:g.3063349G>A GRCh37
NC_000020.9:g.3011349G>A NCBI36
NG_008663.1:g.7022C>T , LRG_715:g.7022C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.422C>T MANE Select ENSP00000369647.3:p.Ala141Val
NM_000490.4:c.422C>T , LRG_715t1:c.422C>T NP_000481.2:p.Ala141Val
XM_011529267.1:c.422C>T XP_011527569.1:p.Ala141Val
XM_011529267.2:c.422C>T XP_011527569.1:p.Ala141Val
NM_000490.5:c.422C>T MANE Select NP_000481.2:p.Ala141Val
Search 100 bp 5'
Search 100 bp 3'