Canonical Allele Identifier: CA408061393
Gene: AVP HGNC NCBI

Linked Data

gnomAD v4: 20-3082775-C-G
MyVariant Identifiers: chr20:g.3063421C>G (hg19) chr20:g.3082775C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3082775C>G , CM000682.2:g.3082775C>G GRCh38
NC_000020.10:g.3063421C>G , CM000682.1:g.3063421C>G GRCh37
NC_000020.9:g.3011421C>G NCBI36
NG_008663.1:g.6950G>C , LRG_715:g.6950G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.350G>C MANE Select ENSP00000369647.3:p.Arg117Pro
NM_000490.4:c.350G>C , LRG_715t1:c.350G>C NP_000481.2:p.Arg117Pro
XM_011529267.1:c.350G>C XP_011527569.1:p.Arg117Pro
XM_011529267.2:c.350G>C XP_011527569.1:p.Arg117Pro
NM_000490.5:c.350G>C MANE Select NP_000481.2:p.Arg117Pro
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