Canonical Allele Identifier: CA509554714

Gene: AVP

Linked Data

• dbSNP Id: rs747554567
• gnomAD v4: 20-3083092-C-A
• MyVariant Identifiers: chr20:g.3063738C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3083092C>A , CM000682.2:g.3083092C>A	GRCh38
NC_000020.10:g.3063738C>A , CM000682.1:g.3063738C>A	GRCh37
NC_000020.9:g.3011738C>A	NCBI36
NG_008663.1:g.6633G>T , LRG_715:g.6633G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000380293.3:c.207G>T MANE Select	ENSP00000369647.3:p.Thr69=
NM_000490.4:c.207G>T , LRG_715t1:c.207G>T	NP_000481.2:p.Thr69=
XM_011529267.1:c.207G>T	XP_011527569.1:p.Thr69=
XM_011529267.2:c.207G>T	XP_011527569.1:p.Thr69=
NM_000490.5:c.207G>T MANE Select	NP_000481.2:p.Thr69=