Canonical Allele Identifier: CA408061639
Gene: AVP HGNC NCBI

Linked Data

dbSNP Id: rs2148570907
gnomAD v4: 20-3083060-T-G
MyVariant Identifiers: chr20:g.3063706T>G (hg19) chr20:g.3083060T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3083060T>G , CM000682.2:g.3083060T>G GRCh38
NC_000020.10:g.3063706T>G , CM000682.1:g.3063706T>G GRCh37
NC_000020.9:g.3011706T>G NCBI36
NG_008663.1:g.6665A>C , LRG_715:g.6665A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.239A>C MANE Select ENSP00000369647.3:p.Tyr80Ser
NM_000490.4:c.239A>C , LRG_715t1:c.239A>C NP_000481.2:p.Tyr80Ser
XM_011529267.1:c.239A>C XP_011527569.1:p.Tyr80Ser
XM_011529267.2:c.239A>C XP_011527569.1:p.Tyr80Ser
NM_000490.5:c.239A>C MANE Select NP_000481.2:p.Tyr80Ser
Search 100 bp 5'
Search 100 bp 3'