Canonical Allele Identifier: CA2651674478

Gene: AVP

Linked Data

• gnomAD v4: 20-3082862-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3082862G>A , CM000682.2:g.3082862G>A	GRCh38
NC_000020.10:g.3063508G>A , CM000682.1:g.3063508G>A	GRCh37
NC_000020.9:g.3011508G>A	NCBI36
NG_008663.1:g.6863C>T , LRG_715:g.6863C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380293.3:c.323-60C>T MANE Select	ENSP00000369647.3:n.323-60C>T
NM_000490.4:c.323-60C>T , LRG_715t1:c.323-60C>T	NP_000481.2:n.323-60C>T
XM_011529267.1:c.323-60C>T	XP_011527569.1:n.323-60C>T
XM_011529267.2:c.323-60C>T	XP_011527569.1:n.323-60C>T
NM_000490.5:c.323-60C>T MANE Select	NP_000481.2:n.323-60C>T