Canonical Allele Identifier: CA2346405401

Gene: AVP

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3082859G= , CM000682.2:g.3082859G=	GRCh38
NC_000020.10:g.3063505G= , CM000682.1:g.3063505G=	GRCh37
NC_000020.9:g.3011505G=	NCBI36
NG_008663.1:g.6866C= , LRG_715:g.6866C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380293.3:c.323-57C= MANE Select	ENSP00000369647.3:n.323-57C=
NM_000490.4:c.323-57C= , LRG_715t1:c.323-57C=	NP_000481.2:n.323-57C=
XM_011529267.1:c.323-57C=	XP_011527569.1:n.323-57C=
XM_011529267.2:c.323-57C=	XP_011527569.1:n.323-57C=
NM_000490.5:c.323-57C= MANE Select	NP_000481.2:n.323-57C=