Canonical Allele Identifier: CA2577323005

Gene: AVP

Linked Data

• gnomAD v4: 20-3082880-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3082880C>A , CM000682.2:g.3082880C>A	GRCh38
NC_000020.10:g.3063526C>A , CM000682.1:g.3063526C>A	GRCh37
NC_000020.9:g.3011526C>A	NCBI36
NG_008663.1:g.6845G>T , LRG_715:g.6845G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380293.3:c.323-78G>T MANE Select	ENSP00000369647.3:n.323-78G>T
NM_000490.4:c.323-78G>T , LRG_715t1:c.323-78G>T	NP_000481.2:n.323-78G>T
XM_011529267.1:c.323-78G>T	XP_011527569.1:n.323-78G>T
XM_011529267.2:c.323-78G>T	XP_011527569.1:n.323-78G>T
NM_000490.5:c.323-78G>T MANE Select	NP_000481.2:n.323-78G>T