Canonical Allele Identifier: CA2346406186
Gene: AVP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3084620C= , CM000682.2:g.3084620C= GRCh38
NC_000020.10:g.3065266C= , CM000682.1:g.3065266C= GRCh37
NC_000020.9:g.3013266C= NCBI36
NG_008663.1:g.5105G= , LRG_715:g.5105G=

Transcript Alleles

HGVS Amino-acid change
ENST00000380293.3:c.55G= MANE Select ENSP00000369647.3:p.Ala19=
NM_000490.4:c.55G= , LRG_715t1:c.55G= NP_000481.2:p.Ala19=
XM_011529267.1:c.55G= XP_011527569.1:p.Ala19=
XM_011529267.2:c.55G= XP_011527569.1:p.Ala19=
NM_000490.5:c.55G= MANE Select NP_000481.2:p.Ala19=