Canonical Allele Identifier: CA2346405961

Gene: AVP

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3084137G= , CM000682.2:g.3084137G=	GRCh38
NC_000020.10:g.3064783G= , CM000682.1:g.3064783G=	GRCh37
NC_000020.9:g.3012783G=	NCBI36
NG_008663.1:g.5588C= , LRG_715:g.5588C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380293.3:c.120+418C= MANE Select	ENSP00000369647.3:n.120+418C=
NM_000490.4:c.120+418C= , LRG_715t1:c.120+418C=	NP_000481.2:n.120+418C=
XM_011529267.1:c.120+418C=	XP_011527569.1:n.120+418C=
XM_011529267.2:c.120+418C=	XP_011527569.1:n.120+418C=
NM_000490.5:c.120+418C= MANE Select	NP_000481.2:n.120+418C=