Canonical Allele Identifier: CA408061366
Gene: AVP HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.3063409T>A (hg19) chr20:g.3082763T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3082763T>A , CM000682.2:g.3082763T>A GRCh38
NC_000020.10:g.3063409T>A , CM000682.1:g.3063409T>A GRCh37
NC_000020.9:g.3011409T>A NCBI36
NG_008663.1:g.6962A>T , LRG_715:g.6962A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.362A>T MANE Select ENSP00000369647.3:p.His121Leu
NM_000490.4:c.362A>T , LRG_715t1:c.362A>T NP_000481.2:p.His121Leu
XM_011529267.1:c.362A>T XP_011527569.1:p.His121Leu
XM_011529267.2:c.362A>T XP_011527569.1:p.His121Leu
NM_000490.5:c.362A>T MANE Select NP_000481.2:p.His121Leu
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