Canonical Allele Identifier: CA2346405207
Gene: AVP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3082690C= , CM000682.2:g.3082690C= GRCh38
NC_000020.10:g.3063336C= , CM000682.1:g.3063336C= GRCh37
NC_000020.9:g.3011336C= NCBI36
NG_008663.1:g.7035G= , LRG_715:g.7035G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.435G= MANE Select ENSP00000369647.3:p.Arg145=
NM_000490.4:c.435G= , LRG_715t1:c.435G= NP_000481.2:p.Arg145=
XM_011529267.1:c.435G= XP_011527569.1:p.Arg145=
XM_011529267.2:c.435G= XP_011527569.1:p.Arg145=
NM_000490.5:c.435G= MANE Select NP_000481.2:p.Arg145=