Canonical Allele Identifier: CA2346405567
Gene: AVP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3083069T= , CM000682.2:g.3083069T= GRCh38
NC_000020.10:g.3063715T= , CM000682.1:g.3063715T= GRCh37
NC_000020.9:g.3011715T= NCBI36
NG_008663.1:g.6656A= , LRG_715:g.6656A=

Transcript Alleles

HGVS Amino-acid change
ENST00000380293.3:c.230A= MANE Select ENSP00000369647.3:p.Glu77=
NM_000490.4:c.230A= , LRG_715t1:c.230A= NP_000481.2:p.Glu77=
XM_011529267.1:c.230A= XP_011527569.1:p.Glu77=
XM_011529267.2:c.230A= XP_011527569.1:p.Glu77=
NM_000490.5:c.230A= MANE Select NP_000481.2:p.Glu77=