Canonical Allele Identifier: CA408062697
Gene: AVP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3084616C>A , CM000682.2:g.3084616C>A GRCh38
NC_000020.10:g.3065262C>A , CM000682.1:g.3065262C>A GRCh37
NC_000020.9:g.3013262C>A NCBI36
NG_008663.1:g.5109G>T , LRG_715:g.5109G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000380293.3:c.59G>T MANE Select ENSP00000369647.3:p.Cys20Phe
NM_000490.4:c.59G>T , LRG_715t1:c.59G>T NP_000481.2:p.Cys20Phe
XM_011529267.1:c.59G>T XP_011527569.1:p.Cys20Phe
XM_011529267.2:c.59G>T XP_011527569.1:p.Cys20Phe
NM_000490.5:c.59G>T MANE Select NP_000481.2:p.Cys20Phe