Canonical Allele Identifier: CA2346406156
Gene: AVP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3084557G= , CM000682.2:g.3084557G= GRCh38
NC_000020.10:g.3065203G= , CM000682.1:g.3065203G= GRCh37
NC_000020.9:g.3013203G= NCBI36
NG_008663.1:g.5168C= , LRG_715:g.5168C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.118C= MANE Select ENSP00000369647.3:p.Gln40=
NM_000490.4:c.118C= , LRG_715t1:c.118C= NP_000481.2:p.Gln40=
XM_011529267.1:c.118C= XP_011527569.1:p.Gln40=
XM_011529267.2:c.118C= XP_011527569.1:p.Gln40=
NM_000490.5:c.118C= MANE Select NP_000481.2:p.Gln40=