Canonical Allele Identifier: CA509554628

Gene: AVP

Linked Data

• gnomAD v4: 20-3082993-G-A
• MyVariant Identifiers: chr20:g.3063639G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3082993G>A , CM000682.2:g.3082993G>A	GRCh38
NC_000020.10:g.3063639G>A , CM000682.1:g.3063639G>A	GRCh37
NC_000020.9:g.3011639G>A	NCBI36
NG_008663.1:g.6732C>T , LRG_715:g.6732C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380293.3:c.306C>T MANE Select	ENSP00000369647.3:p.Gly102=
NM_000490.4:c.306C>T , LRG_715t1:c.306C>T	NP_000481.2:p.Gly102=
XM_011529267.1:c.306C>T	XP_011527569.1:p.Gly102=
XM_011529267.2:c.306C>T	XP_011527569.1:p.Gly102=
NM_000490.5:c.306C>T MANE Select	NP_000481.2:p.Gly102=