Canonical Allele Identifier: CA310942877
Gene: AVP HGNC NCBI

Linked Data

ClinVar Variation Id: 2179297
ClinVar RCV Id: RCV002615089
dbSNP Id: rs1044716891
gnomAD v2: 20-3063338-G-T
gnomAD v3: 20-3082692-G-T
gnomAD v4: 20-3082692-G-T
MyVariant Identifiers: chr20:g.3063338G>T (hg19) chr20:g.3082692G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3082692G>T , CM000682.2:g.3082692G>T GRCh38
NC_000020.10:g.3063338G>T , CM000682.1:g.3063338G>T GRCh37
NC_000020.9:g.3011338G>T NCBI36
NG_008663.1:g.7033C>A , LRG_715:g.7033C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.433C>A MANE Select ENSP00000369647.3:p.Arg145=
NM_000490.4:c.433C>A , LRG_715t1:c.433C>A NP_000481.2:p.Arg145=
XM_011529267.1:c.433C>A XP_011527569.1:p.Arg145=
XM_011529267.2:c.433C>A XP_011527569.1:p.Arg145=
NM_000490.5:c.433C>A MANE Select NP_000481.2:p.Arg145=
Search 100 bp 5'
Search 100 bp 3'