Canonical Allele Identifier: CA2346405599
Gene: AVP HGNC NCBI

Linked Data

dbSNP Id: rs2066120212
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3083155del , CM000682.2:g.3083155del GRCh38
NC_000020.10:g.3063801del , CM000682.1:g.3063801del GRCh37
NC_000020.9:g.3011801del NCBI36
NG_008663.1:g.6570del , LRG_715:g.6570del

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.144del MANE Select ENSP00000369647.3:p.Gly50AlafsTer?
NM_000490.4:c.144del , LRG_715t1:c.144del NP_000481.2:p.Gly50AlafsTer?
XM_011529267.1:c.144del XP_011527569.1:p.Gly50AlafsTer?
XM_011529267.2:c.144del XP_011527569.1:p.Gly50AlafsTer?
NM_000490.5:c.144del MANE Select NP_000481.2:p.Gly50AlafsTer?
Search 100 bp 5'
Search 100 bp 3'