Canonical Allele Identifier: CA2346405612

Gene: AVP

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3083169A= , CM000682.2:g.3083169A=	GRCh38
NC_000020.10:g.3063815A= , CM000682.1:g.3063815A=	GRCh37
NC_000020.9:g.3011815A=	NCBI36
NG_008663.1:g.6556T= , LRG_715:g.6556T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380293.3:c.130T= MANE Select	ENSP00000369647.3:p.Cys44=
NM_000490.4:c.130T= , LRG_715t1:c.130T=	NP_000481.2:p.Cys44=
XM_011529267.1:c.130T=	XP_011527569.1:p.Cys44=
XM_011529267.2:c.130T=	XP_011527569.1:p.Cys44=
NM_000490.5:c.130T= MANE Select	NP_000481.2:p.Cys44=