Canonical Allele Identifier: CA2651675062

Gene: AVP

Linked Data

• gnomAD v4: 20-3084423-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3084423C>G , CM000682.2:g.3084423C>G	GRCh38
NC_000020.10:g.3065069C>G , CM000682.1:g.3065069C>G	GRCh37
NC_000020.9:g.3013069C>G	NCBI36
NG_008663.1:g.5302G>C , LRG_715:g.5302G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380293.3:c.120+132G>C MANE Select	ENSP00000369647.3:n.120+132G>C
NM_000490.4:c.120+132G>C , LRG_715t1:c.120+132G>C	NP_000481.2:n.120+132G>C
XM_011529267.1:c.120+132G>C	XP_011527569.1:n.120+132G>C
XM_011529267.2:c.120+132G>C	XP_011527569.1:n.120+132G>C
NM_000490.5:c.120+132G>C MANE Select	NP_000481.2:n.120+132G>C