Canonical Allele Identifier: CA2577323000
Gene: AVP HGNC NCBI

Linked Data

gnomAD v4: 20-3082830-GC-G
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3082833del , CM000682.2:g.3082833del GRCh38
NC_000020.10:g.3063479del , CM000682.1:g.3063479del GRCh37
NC_000020.9:g.3011479del NCBI36
NG_008663.1:g.6894del , LRG_715:g.6894del

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.323-29del MANE Select ENSP00000369647.3:n.323-29del
NM_000490.4:c.323-29del , LRG_715t1:c.323-29del NP_000481.2:n.323-29del
XM_011529267.1:c.323-29del XP_011527569.1:n.323-29del
XM_011529267.2:c.323-29del XP_011527569.1:n.323-29del
NM_000490.5:c.323-29del MANE Select NP_000481.2:n.323-29del
Search 100 bp 5'
Search 100 bp 3'