Canonical Allele Identifier: CA2651674389
Gene: AVP HGNC NCBI

Linked Data

gnomAD v4: 20-3082810-G-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3082810G>A , CM000682.2:g.3082810G>A GRCh38
NC_000020.10:g.3063456G>A , CM000682.1:g.3063456G>A GRCh37
NC_000020.9:g.3011456G>A NCBI36
NG_008663.1:g.6915C>T , LRG_715:g.6915C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.323-8C>T MANE Select ENSP00000369647.3:n.323-8C>T
NM_000490.4:c.323-8C>T , LRG_715t1:c.323-8C>T NP_000481.2:n.323-8C>T
XM_011529267.1:c.323-8C>T XP_011527569.1:n.323-8C>T
XM_011529267.2:c.323-8C>T XP_011527569.1:n.323-8C>T
NM_000490.5:c.323-8C>T MANE Select NP_000481.2:n.323-8C>T
Search 100 bp 5'
Search 100 bp 3'