Canonical Allele Identifier: CA2346405251
Gene: AVP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3082721A= , CM000682.2:g.3082721A= GRCh38
NC_000020.10:g.3063367A= , CM000682.1:g.3063367A= GRCh37
NC_000020.9:g.3011367A= NCBI36
NG_008663.1:g.7004T= , LRG_715:g.7004T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.404T= MANE Select ENSP00000369647.3:p.Leu135=
NM_000490.4:c.404T= , LRG_715t1:c.404T= NP_000481.2:p.Leu135=
XM_011529267.1:c.404T= XP_011527569.1:p.Leu135=
XM_011529267.2:c.404T= XP_011527569.1:p.Leu135=
NM_000490.5:c.404T= MANE Select NP_000481.2:p.Leu135=