Canonical Allele Identifier: CA634328992

Gene: AVP

Linked Data

• dbSNP Id: rs762655956
• gnomAD v2: 20-3063591-C-CT
• gnomAD v3: 20-3082945-C-CT
• gnomAD v4: 20-3082945-C-CT
• MyVariant Identifiers: chr20:g.3063591_3063592insT (hg19) ; chr20:g.3082945_3082946insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3082945_3082946insT , CM000682.2:g.3082945_3082946insT	GRCh38
NC_000020.10:g.3063591_3063592insT , CM000682.1:g.3063591_3063592insT	GRCh37
NC_000020.9:g.3011591_3011592insT	NCBI36
NG_008663.1:g.6779_6780insA , LRG_715:g.6779_6780insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380293.3:c.322+31_322+32insA MANE Select	ENSP00000369647.3:n.322+31_322+32insA
NM_000490.4:c.322+31_322+32insA , LRG_715t1:c.322+31_322+32insA	NP_000481.2:n.322+31_322+32insA
XM_011529267.1:c.322+31_322+32insA	XP_011527569.1:n.322+31_322+32insA
XM_011529267.2:c.322+31_322+32insA	XP_011527569.1:n.322+31_322+32insA
NM_000490.5:c.322+31_322+32insA MANE Select	NP_000481.2:n.322+31_322+32insA