Canonical Allele Identifier: CA2697547264
Gene: AVP HGNC NCBI

Linked Data

ClinVar Variation Id: 2705624
ClinVar RCV Id: RCV003575522
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3082814A>C , CM000682.2:g.3082814A>C GRCh38
NC_000020.10:g.3063460A>C , CM000682.1:g.3063460A>C GRCh37
NC_000020.9:g.3011460A>C NCBI36
NG_008663.1:g.6911T>G , LRG_715:g.6911T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.323-12T>G MANE Select ENSP00000369647.3:n.323-12T>G
NM_000490.4:c.323-12T>G , LRG_715t1:c.323-12T>G NP_000481.2:n.323-12T>G
XM_011529267.1:c.323-12T>G XP_011527569.1:n.323-12T>G
XM_011529267.2:c.323-12T>G XP_011527569.1:n.323-12T>G
NM_000490.5:c.323-12T>G MANE Select NP_000481.2:n.323-12T>G
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