Canonical Allele Identifier: CA408062767

Gene: AVP

Linked Data

• MyVariant Identifiers: chr20:g.3065275A>C (hg19) ; chr20:g.3084629A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3084629A>C , CM000682.2:g.3084629A>C	GRCh38
NC_000020.10:g.3065275A>C , CM000682.1:g.3065275A>C	GRCh37
NC_000020.9:g.3013275A>C	NCBI36
NG_008663.1:g.5096T>G , LRG_715:g.5096T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380293.3:c.46T>G MANE Select	ENSP00000369647.3:p.Phe16Val
NM_000490.4:c.46T>G , LRG_715t1:c.46T>G	NP_000481.2:p.Phe16Val
XM_011529267.1:c.46T>G	XP_011527569.1:p.Phe16Val
XM_011529267.2:c.46T>G	XP_011527569.1:p.Phe16Val
NM_000490.5:c.46T>G MANE Select	NP_000481.2:p.Phe16Val