Canonical Allele Identifier: CA2346405255
Gene: AVP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3082722G= , CM000682.2:g.3082722G= GRCh38
NC_000020.10:g.3063368G= , CM000682.1:g.3063368G= GRCh37
NC_000020.9:g.3011368G= NCBI36
NG_008663.1:g.7003C= , LRG_715:g.7003C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.403C= MANE Select ENSP00000369647.3:p.Leu135=
NM_000490.4:c.403C= , LRG_715t1:c.403C= NP_000481.2:p.Leu135=
XM_011529267.1:c.403C= XP_011527569.1:p.Leu135=
XM_011529267.2:c.403C= XP_011527569.1:p.Leu135=
NM_000490.5:c.403C= MANE Select NP_000481.2:p.Leu135=