Canonical Allele Identifier: CA2346405357
Gene: AVP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3082802T= , CM000682.2:g.3082802T= GRCh38
NC_000020.10:g.3063448T= , CM000682.1:g.3063448T= GRCh37
NC_000020.9:g.3011448T= NCBI36
NG_008663.1:g.6923A= , LRG_715:g.6923A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.323A= MANE Select ENSP00000369647.3:p.Glu108=
NM_000490.4:c.323A= , LRG_715t1:c.323A= NP_000481.2:p.Glu108=
XM_011529267.1:c.323A= XP_011527569.1:p.Glu108=
XM_011529267.2:c.323A= XP_011527569.1:p.Glu108=
NM_000490.5:c.323A= MANE Select NP_000481.2:p.Glu108=