Canonical Allele Identifier: CA2346406113
Gene: AVP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3084459A= , CM000682.2:g.3084459A= GRCh38
NC_000020.10:g.3065105A= , CM000682.1:g.3065105A= GRCh37
NC_000020.9:g.3013105A= NCBI36
NG_008663.1:g.5266T= , LRG_715:g.5266T=

Transcript Alleles

HGVS Amino-acid change
ENST00000380293.3:c.120+96T= MANE Select ENSP00000369647.3:n.120+96T=
NM_000490.4:c.120+96T= , LRG_715t1:c.120+96T= NP_000481.2:n.120+96T=
XM_011529267.1:c.120+96T= XP_011527569.1:n.120+96T=
XM_011529267.2:c.120+96T= XP_011527569.1:n.120+96T=
NM_000490.5:c.120+96T= MANE Select NP_000481.2:n.120+96T=
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