Canonical Allele Identifier: CA408061664
Gene: AVP HGNC NCBI

Linked Data

gnomAD v4: 20-3083070-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3083070C>T , CM000682.2:g.3083070C>T GRCh38
NC_000020.10:g.3063716C>T , CM000682.1:g.3063716C>T GRCh37
NC_000020.9:g.3011716C>T NCBI36
NG_008663.1:g.6655G>A , LRG_715:g.6655G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000380293.3:c.229G>A MANE Select ENSP00000369647.3:p.Glu77Lys
NM_000490.4:c.229G>A , LRG_715t1:c.229G>A NP_000481.2:p.Glu77Lys
XM_011529267.1:c.229G>A XP_011527569.1:p.Glu77Lys
XM_011529267.2:c.229G>A XP_011527569.1:p.Glu77Lys
NM_000490.5:c.229G>A MANE Select NP_000481.2:p.Glu77Lys