Canonical Allele Identifier: CA743331271
Gene: AVP HGNC NCBI

Linked Data

dbSNP Id: rs1338659044
gnomAD v3: 20-3084149-C-T
gnomAD v4: 20-3084149-C-T
MyVariant Identifiers: chr20:g.3064795C>T (hg19) chr20:g.3084149C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3084149C>T , CM000682.2:g.3084149C>T GRCh38
NC_000020.10:g.3064795C>T , CM000682.1:g.3064795C>T GRCh37
NC_000020.9:g.3012795C>T NCBI36
NG_008663.1:g.5576G>A , LRG_715:g.5576G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.120+406G>A MANE Select ENSP00000369647.3:n.120+406G>A
NM_000490.4:c.120+406G>A , LRG_715t1:c.120+406G>A NP_000481.2:n.120+406G>A
XM_011529267.1:c.120+406G>A XP_011527569.1:n.120+406G>A
XM_011529267.2:c.120+406G>A XP_011527569.1:n.120+406G>A
NM_000490.5:c.120+406G>A MANE Select NP_000481.2:n.120+406G>A
Search 100 bp 5'
Search 100 bp 3'