Canonical Allele Identifier: CA2548913084
Gene: AVP HGNC NCBI

Linked Data

gnomAD v4: 20-3082857-CG-C
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3082863del , CM000682.2:g.3082863del GRCh38
NC_000020.10:g.3063509del , CM000682.1:g.3063509del GRCh37
NC_000020.9:g.3011509del NCBI36
NG_008663.1:g.6867del , LRG_715:g.6867del

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.323-56del MANE Select ENSP00000369647.3:n.323-56del
NM_000490.4:c.323-56del , LRG_715t1:c.323-56del NP_000481.2:n.323-56del
XM_011529267.1:c.323-56del XP_011527569.1:n.323-56del
XM_011529267.2:c.323-56del XP_011527569.1:n.323-56del
NM_000490.5:c.323-56del MANE Select NP_000481.2:n.323-56del
Search 100 bp 5'
Search 100 bp 3'