Canonical Allele Identifier: CA509404353
Gene: AVP HGNC NCBI

Linked Data

gnomAD v4: 20-3082768-G-C
MyVariant Identifiers: chr20:g.3063414G>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3082768G>C , CM000682.2:g.3082768G>C GRCh38
NC_000020.10:g.3063414G>C , CM000682.1:g.3063414G>C GRCh37
NC_000020.9:g.3011414G>C NCBI36
NG_008663.1:g.6957C>G , LRG_715:g.6957C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.357C>G MANE Select ENSP00000369647.3:p.Gly119=
NM_000490.4:c.357C>G , LRG_715t1:c.357C>G NP_000481.2:p.Gly119=
XM_011529267.1:c.357C>G XP_011527569.1:p.Gly119=
XM_011529267.2:c.357C>G XP_011527569.1:p.Gly119=
NM_000490.5:c.357C>G MANE Select NP_000481.2:p.Gly119=
Search 100 bp 5'
Search 100 bp 3'