Canonical Allele Identifier: CA408061679
Gene: AVP HGNC NCBI

Linked Data

gnomAD v4: 20-3083076-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3083076A>G , CM000682.2:g.3083076A>G GRCh38
NC_000020.10:g.3063722A>G , CM000682.1:g.3063722A>G GRCh37
NC_000020.9:g.3011722A>G NCBI36
NG_008663.1:g.6649T>C , LRG_715:g.6649T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000380293.3:c.223T>C MANE Select ENSP00000369647.3:p.Cys75Arg
NM_000490.4:c.223T>C , LRG_715t1:c.223T>C NP_000481.2:p.Cys75Arg
XM_011529267.1:c.223T>C XP_011527569.1:p.Cys75Arg
XM_011529267.2:c.223T>C XP_011527569.1:p.Cys75Arg
NM_000490.5:c.223T>C MANE Select NP_000481.2:p.Cys75Arg