Canonical Allele Identifier: CA2651675059

Gene: AVP

Linked Data

• gnomAD v4: 20-3084418-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3084418C>T , CM000682.2:g.3084418C>T	GRCh38
NC_000020.10:g.3065064C>T , CM000682.1:g.3065064C>T	GRCh37
NC_000020.9:g.3013064C>T	NCBI36
NG_008663.1:g.5307G>A , LRG_715:g.5307G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000380293.3:c.120+137G>A MANE Select	ENSP00000369647.3:n.120+137G>A
NM_000490.4:c.120+137G>A , LRG_715t1:c.120+137G>A	NP_000481.2:n.120+137G>A
XM_011529267.1:c.120+137G>A	XP_011527569.1:n.120+137G>A
XM_011529267.2:c.120+137G>A	XP_011527569.1:n.120+137G>A
NM_000490.5:c.120+137G>A MANE Select	NP_000481.2:n.120+137G>A