Canonical Allele Identifier: CA2346405955

Gene: AVP

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3084132T= , CM000682.2:g.3084132T=	GRCh38
NC_000020.10:g.3064778T= , CM000682.1:g.3064778T=	GRCh37
NC_000020.9:g.3012778T=	NCBI36
NG_008663.1:g.5593A= , LRG_715:g.5593A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380293.3:c.120+423A= MANE Select	ENSP00000369647.3:n.120+423A=
NM_000490.4:c.120+423A= , LRG_715t1:c.120+423A=	NP_000481.2:n.120+423A=
XM_011529267.1:c.120+423A=	XP_011527569.1:n.120+423A=
XM_011529267.2:c.120+423A=	XP_011527569.1:n.120+423A=
NM_000490.5:c.120+423A= MANE Select	NP_000481.2:n.120+423A=