Canonical Allele Identifier: CA408062368

Gene: AVP

Linked Data

• MyVariant Identifiers: chr20:g.3065199A>T (hg19) ; chr20:g.3084553A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3084553A>T , CM000682.2:g.3084553A>T	GRCh38
NC_000020.10:g.3065199A>T , CM000682.1:g.3065199A>T	GRCh37
NC_000020.9:g.3013199A>T	NCBI36
NG_008663.1:g.5172T>A , LRG_715:g.5172T>A

Transcript Alleles

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