Canonical Allele Identifier: CA408061225
Gene: AVP HGNC NCBI

Linked Data

dbSNP Id: rs936650522
gnomAD v3: 20-3082691-C-T
gnomAD v4: 20-3082691-C-T
MyVariant Identifiers: chr20:g.3063337C>T (hg19) chr20:g.3082691C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3082691C>T , CM000682.2:g.3082691C>T GRCh38
NC_000020.10:g.3063337C>T , CM000682.1:g.3063337C>T GRCh37
NC_000020.9:g.3011337C>T NCBI36
NG_008663.1:g.7034G>A , LRG_715:g.7034G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.434G>A MANE Select ENSP00000369647.3:p.Arg145Gln
NM_000490.4:c.434G>A , LRG_715t1:c.434G>A NP_000481.2:p.Arg145Gln
XM_011529267.1:c.434G>A XP_011527569.1:p.Arg145Gln
XM_011529267.2:c.434G>A XP_011527569.1:p.Arg145Gln
NM_000490.5:c.434G>A MANE Select NP_000481.2:p.Arg145Gln
Search 100 bp 5'
Search 100 bp 3'