Canonical Allele Identifier: CA2346405232
Gene: AVP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3082708G= , CM000682.2:g.3082708G= GRCh38
NC_000020.10:g.3063354G= , CM000682.1:g.3063354G= GRCh37
NC_000020.9:g.3011354G= NCBI36
NG_008663.1:g.7017C= , LRG_715:g.7017C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.417C= MANE Select ENSP00000369647.3:p.Ala139=
NM_000490.4:c.417C= , LRG_715t1:c.417C= NP_000481.2:p.Ala139=
XM_011529267.1:c.417C= XP_011527569.1:p.Ala139=
XM_011529267.2:c.417C= XP_011527569.1:p.Ala139=
NM_000490.5:c.417C= MANE Select NP_000481.2:p.Ala139=