Canonical Allele Identifier: CA509404227
Gene: AVP HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.3063384C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3082738C>G , CM000682.2:g.3082738C>G GRCh38
NC_000020.10:g.3063384C>G , CM000682.1:g.3063384C>G GRCh37
NC_000020.9:g.3011384C>G NCBI36
NG_008663.1:g.6987G>C , LRG_715:g.6987G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.387G>C MANE Select ENSP00000369647.3:p.Arg129=
NM_000490.4:c.387G>C , LRG_715t1:c.387G>C NP_000481.2:p.Arg129=
XM_011529267.1:c.387G>C XP_011527569.1:p.Arg129=
XM_011529267.2:c.387G>C XP_011527569.1:p.Arg129=
NM_000490.5:c.387G>C MANE Select NP_000481.2:p.Arg129=
Search 100 bp 5'
Search 100 bp 3'