Canonical Allele Identifier: CA408061449
Gene: AVP HGNC NCBI

Linked Data

gnomAD v4: 20-3082802-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3082802T>C , CM000682.2:g.3082802T>C GRCh38
NC_000020.10:g.3063448T>C , CM000682.1:g.3063448T>C GRCh37
NC_000020.9:g.3011448T>C NCBI36
NG_008663.1:g.6923A>G , LRG_715:g.6923A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.323A>G MANE Select ENSP00000369647.3:p.Glu108Gly
NM_000490.4:c.323A>G , LRG_715t1:c.323A>G NP_000481.2:p.Glu108Gly
XM_011529267.1:c.323A>G XP_011527569.1:p.Glu108Gly
XM_011529267.2:c.323A>G XP_011527569.1:p.Glu108Gly
NM_000490.5:c.323A>G MANE Select NP_000481.2:p.Glu108Gly