Canonical Allele Identifier: CA408061260
Gene: AVP HGNC NCBI

Linked Data

gnomAD v4: 20-3082712-G-T
MyVariant Identifiers: chr20:g.3063358G>T (hg19) chr20:g.3082712G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3082712G>T , CM000682.2:g.3082712G>T GRCh38
NC_000020.10:g.3063358G>T , CM000682.1:g.3063358G>T GRCh37
NC_000020.9:g.3011358G>T NCBI36
NG_008663.1:g.7013C>A , LRG_715:g.7013C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.413C>A MANE Select ENSP00000369647.3:p.Pro138Gln
NM_000490.4:c.413C>A , LRG_715t1:c.413C>A NP_000481.2:p.Pro138Gln
XM_011529267.1:c.413C>A XP_011527569.1:p.Pro138Gln
XM_011529267.2:c.413C>A XP_011527569.1:p.Pro138Gln
NM_000490.5:c.413C>A MANE Select NP_000481.2:p.Pro138Gln
Search 100 bp 5'
Search 100 bp 3'