Canonical Allele Identifier: CA2577323041
Gene: AVP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3084461C>G , CM000682.2:g.3084461C>G GRCh38
NC_000020.10:g.3065107C>G , CM000682.1:g.3065107C>G GRCh37
NC_000020.9:g.3013107C>G NCBI36
NG_008663.1:g.5264G>C , LRG_715:g.5264G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000380293.3:c.120+94G>C MANE Select ENSP00000369647.3:n.120+94G>C
NM_000490.4:c.120+94G>C , LRG_715t1:c.120+94G>C NP_000481.2:n.120+94G>C
XM_011529267.1:c.120+94G>C XP_011527569.1:n.120+94G>C
XM_011529267.2:c.120+94G>C XP_011527569.1:n.120+94G>C
NM_000490.5:c.120+94G>C MANE Select NP_000481.2:n.120+94G>C