Canonical Allele Identifier: CA2346406029
Gene: AVP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3084268C= , CM000682.2:g.3084268C= GRCh38
NC_000020.10:g.3064914C= , CM000682.1:g.3064914C= GRCh37
NC_000020.9:g.3012914C= NCBI36
NG_008663.1:g.5457G= , LRG_715:g.5457G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.120+287G= MANE Select ENSP00000369647.3:n.120+287G=
NM_000490.4:c.120+287G= , LRG_715t1:c.120+287G= NP_000481.2:n.120+287G=
XM_011529267.1:c.120+287G= XP_011527569.1:n.120+287G=
XM_011529267.2:c.120+287G= XP_011527569.1:n.120+287G=
NM_000490.5:c.120+287G= MANE Select NP_000481.2:n.120+287G=