Canonical Allele Identifier: CA408061588

Gene: AVP

Linked Data

• gnomAD v4: 20-3083036-C-G
• MyVariant Identifiers: chr20:g.3063682C>G (hg19) ; chr20:g.3083036C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3083036C>G , CM000682.2:g.3083036C>G	GRCh38
NC_000020.10:g.3063682C>G , CM000682.1:g.3063682C>G	GRCh37
NC_000020.9:g.3011682C>G	NCBI36
NG_008663.1:g.6689G>C , LRG_715:g.6689G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380293.3:c.263G>C MANE Select	ENSP00000369647.3:p.Gly88Ala
NM_000490.4:c.263G>C , LRG_715t1:c.263G>C	NP_000481.2:p.Gly88Ala
XM_011529267.1:c.263G>C	XP_011527569.1:p.Gly88Ala
XM_011529267.2:c.263G>C	XP_011527569.1:p.Gly88Ala
NM_000490.5:c.263G>C MANE Select	NP_000481.2:p.Gly88Ala