Canonical Allele Identifier: CA2346406111
Gene: AVP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3084449C= , CM000682.2:g.3084449C= GRCh38
NC_000020.10:g.3065095C= , CM000682.1:g.3065095C= GRCh37
NC_000020.9:g.3013095C= NCBI36
NG_008663.1:g.5276G= , LRG_715:g.5276G=

Transcript Alleles

HGVS Amino-acid change
ENST00000380293.3:c.120+106G= MANE Select ENSP00000369647.3:n.120+106G=
NM_000490.4:c.120+106G= , LRG_715t1:c.120+106G= NP_000481.2:n.120+106G=
XM_011529267.1:c.120+106G= XP_011527569.1:n.120+106G=
XM_011529267.2:c.120+106G= XP_011527569.1:n.120+106G=
NM_000490.5:c.120+106G= MANE Select NP_000481.2:n.120+106G=
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