Canonical Allele Identifier: CA2346405501
Gene: AVP HGNC NCBI

Linked Data

dbSNP Id: rs2066118578

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3082950dup , CM000682.2:g.3082950dup GRCh38
NC_000020.10:g.3063596dup , CM000682.1:g.3063596dup GRCh37
NC_000020.9:g.3011596dup NCBI36
NG_008663.1:g.6775dup , LRG_715:g.6775dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.322+27dup MANE Select ENSP00000369647.3:n.322+27dup
NM_000490.4:c.322+27dup , LRG_715t1:c.322+27dup NP_000481.2:n.322+27dup
XM_011529267.1:c.322+27dup XP_011527569.1:n.322+27dup
XM_011529267.2:c.322+27dup XP_011527569.1:n.322+27dup
NM_000490.5:c.322+27dup MANE Select NP_000481.2:n.322+27dup