Canonical Allele Identifier: CA2346405430
Gene: AVP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3082890G= , CM000682.2:g.3082890G= GRCh38
NC_000020.10:g.3063536G= , CM000682.1:g.3063536G= GRCh37
NC_000020.9:g.3011536G= NCBI36
NG_008663.1:g.6835C= , LRG_715:g.6835C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.323-88C= MANE Select ENSP00000369647.3:n.323-88C=
NM_000490.4:c.323-88C= , LRG_715t1:c.323-88C= NP_000481.2:n.323-88C=
XM_011529267.1:c.323-88C= XP_011527569.1:n.323-88C=
XM_011529267.2:c.323-88C= XP_011527569.1:n.323-88C=
NM_000490.5:c.323-88C= MANE Select NP_000481.2:n.323-88C=