Canonical Allele Identifier: CA408061818
Gene: AVP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3083142A>C , CM000682.2:g.3083142A>C GRCh38
NC_000020.10:g.3063788A>C , CM000682.1:g.3063788A>C GRCh37
NC_000020.9:g.3011788A>C NCBI36
NG_008663.1:g.6583T>G , LRG_715:g.6583T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.157T>G MANE Select ENSP00000369647.3:p.Phe53Val
NM_000490.4:c.157T>G , LRG_715t1:c.157T>G NP_000481.2:p.Phe53Val
XM_011529267.1:c.157T>G XP_011527569.1:p.Phe53Val
XM_011529267.2:c.157T>G XP_011527569.1:p.Phe53Val
NM_000490.5:c.157T>G MANE Select NP_000481.2:p.Phe53Val