Canonical Allele Identifier: CA509554629
Gene: AVP HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.3063639G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3082993G>C , CM000682.2:g.3082993G>C GRCh38
NC_000020.10:g.3063639G>C , CM000682.1:g.3063639G>C GRCh37
NC_000020.9:g.3011639G>C NCBI36
NG_008663.1:g.6732C>G , LRG_715:g.6732C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000380293.3:c.306C>G MANE Select ENSP00000369647.3:p.Gly102=
NM_000490.4:c.306C>G , LRG_715t1:c.306C>G NP_000481.2:p.Gly102=
XM_011529267.1:c.306C>G XP_011527569.1:p.Gly102=
XM_011529267.2:c.306C>G XP_011527569.1:p.Gly102=
NM_000490.5:c.306C>G MANE Select NP_000481.2:p.Gly102=
Search 100 bp 5'
Search 100 bp 3'