Canonical Allele Identifier: CA509404257
Gene: AVP HGNC NCBI

Linked Data

gnomAD v4: 20-3082747-G-C
MyVariant Identifiers: chr20:g.3063393G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3082747G>C , CM000682.2:g.3082747G>C GRCh38
NC_000020.10:g.3063393G>C , CM000682.1:g.3063393G>C GRCh37
NC_000020.9:g.3011393G>C NCBI36
NG_008663.1:g.6978C>G , LRG_715:g.6978C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.378C>G MANE Select ENSP00000369647.3:p.Ala126=
NM_000490.4:c.378C>G , LRG_715t1:c.378C>G NP_000481.2:p.Ala126=
XM_011529267.1:c.378C>G XP_011527569.1:p.Ala126=
XM_011529267.2:c.378C>G XP_011527569.1:p.Ala126=
NM_000490.5:c.378C>G MANE Select NP_000481.2:p.Ala126=
Search 100 bp 5'
Search 100 bp 3'