Canonical Allele Identifier: CA408061259
Gene: AVP HGNC NCBI

Linked Data

dbSNP Id: rs1358991807
gnomAD v4: 20-3082712-G-A
MyVariant Identifiers: chr20:g.3063358G>A (hg19) chr20:g.3082712G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3082712G>A , CM000682.2:g.3082712G>A GRCh38
NC_000020.10:g.3063358G>A , CM000682.1:g.3063358G>A GRCh37
NC_000020.9:g.3011358G>A NCBI36
NG_008663.1:g.7013C>T , LRG_715:g.7013C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.413C>T MANE Select ENSP00000369647.3:p.Pro138Leu
NM_000490.4:c.413C>T , LRG_715t1:c.413C>T NP_000481.2:p.Pro138Leu
XM_011529267.1:c.413C>T XP_011527569.1:p.Pro138Leu
XM_011529267.2:c.413C>T XP_011527569.1:p.Pro138Leu
NM_000490.5:c.413C>T MANE Select NP_000481.2:p.Pro138Leu
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