Canonical Allele Identifier: CA634328934
Gene: AVP HGNC NCBI

Linked Data

dbSNP Id: rs1364748075
gnomAD v2: 20-3063873-G-A
gnomAD v3: 20-3083227-G-A
gnomAD v4: 20-3083227-G-A
MyVariant Identifiers: chr20:g.3063873G>A (hg19) chr20:g.3083227G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3083227G>A , CM000682.2:g.3083227G>A GRCh38
NC_000020.10:g.3063873G>A , CM000682.1:g.3063873G>A GRCh37
NC_000020.9:g.3011873G>A NCBI36
NG_008663.1:g.6498C>T , LRG_715:g.6498C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.121-49C>T MANE Select ENSP00000369647.3:n.121-49C>T
NM_000490.4:c.121-49C>T , LRG_715t1:c.121-49C>T NP_000481.2:n.121-49C>T
XM_011529267.1:c.121-49C>T XP_011527569.1:n.121-49C>T
XM_011529267.2:c.121-49C>T XP_011527569.1:n.121-49C>T
NM_000490.5:c.121-49C>T MANE Select NP_000481.2:n.121-49C>T
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