Canonical Allele Identifier: CA509554569
Gene: AVP HGNC NCBI

Linked Data

gnomAD v4: 20-3082789-G-T
MyVariant Identifiers: chr20:g.3063435G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3082789G>T , CM000682.2:g.3082789G>T GRCh38
NC_000020.10:g.3063435G>T , CM000682.1:g.3063435G>T GRCh37
NC_000020.9:g.3011435G>T NCBI36
NG_008663.1:g.6936C>A , LRG_715:g.6936C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.336C>A MANE Select ENSP00000369647.3:p.Thr112=
NM_000490.4:c.336C>A , LRG_715t1:c.336C>A NP_000481.2:p.Thr112=
XM_011529267.1:c.336C>A XP_011527569.1:p.Thr112=
XM_011529267.2:c.336C>A XP_011527569.1:p.Thr112=
NM_000490.5:c.336C>A MANE Select NP_000481.2:p.Thr112=
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