Canonical Allele Identifier: CA408061700
Gene: AVP HGNC NCBI

Linked Data

gnomAD v4: 20-3083087-T-C
MyVariant Identifiers: chr20:g.3063733T>C (hg19) chr20:g.3083087T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3083087T>C , CM000682.2:g.3083087T>C GRCh38
NC_000020.10:g.3063733T>C , CM000682.1:g.3063733T>C GRCh37
NC_000020.9:g.3011733T>C NCBI36
NG_008663.1:g.6638A>G , LRG_715:g.6638A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.212A>G MANE Select ENSP00000369647.3:p.Glu71Gly
NM_000490.4:c.212A>G , LRG_715t1:c.212A>G NP_000481.2:p.Glu71Gly
XM_011529267.1:c.212A>G XP_011527569.1:p.Glu71Gly
XM_011529267.2:c.212A>G XP_011527569.1:p.Glu71Gly
NM_000490.5:c.212A>G MANE Select NP_000481.2:p.Glu71Gly
Search 100 bp 5'
Search 100 bp 3'