Canonical Allele Identifier: CA509554704
Gene: AVP HGNC NCBI

Linked Data

gnomAD v4: 20-3083083-C-A
MyVariant Identifiers: chr20:g.3063729C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3083083C>A , CM000682.2:g.3083083C>A GRCh38
NC_000020.10:g.3063729C>A , CM000682.1:g.3063729C>A GRCh37
NC_000020.9:g.3011729C>A NCBI36
NG_008663.1:g.6642G>T , LRG_715:g.6642G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.216G>T MANE Select ENSP00000369647.3:p.Ala72=
NM_000490.4:c.216G>T , LRG_715t1:c.216G>T NP_000481.2:p.Ala72=
XM_011529267.1:c.216G>T XP_011527569.1:p.Ala72=
XM_011529267.2:c.216G>T XP_011527569.1:p.Ala72=
NM_000490.5:c.216G>T MANE Select NP_000481.2:p.Ala72=