Canonical Allele Identifier: CA2651674532

Gene: AVP

Linked Data

• gnomAD v4: 20-3082893-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3082893G>C , CM000682.2:g.3082893G>C	GRCh38
NC_000020.10:g.3063539G>C , CM000682.1:g.3063539G>C	GRCh37
NC_000020.9:g.3011539G>C	NCBI36
NG_008663.1:g.6832C>G , LRG_715:g.6832C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380293.3:c.322+84C>G MANE Select	ENSP00000369647.3:n.322+84C>G
NM_000490.4:c.322+84C>G , LRG_715t1:c.322+84C>G	NP_000481.2:n.322+84C>G
XM_011529267.1:c.322+84C>G	XP_011527569.1:n.322+84C>G
XM_011529267.2:c.322+84C>G	XP_011527569.1:n.322+84C>G
NM_000490.5:c.322+84C>G MANE Select	NP_000481.2:n.322+84C>G