Canonical Allele Identifier: CA408061268
Gene: AVP HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.3063363G>C (hg19) chr20:g.3082717G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3082717G>C , CM000682.2:g.3082717G>C GRCh38
NC_000020.10:g.3063363G>C , CM000682.1:g.3063363G>C GRCh37
NC_000020.9:g.3011363G>C NCBI36
NG_008663.1:g.7008C>G , LRG_715:g.7008C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.408C>G MANE Select ENSP00000369647.3:p.Asp136Glu
NM_000490.4:c.408C>G , LRG_715t1:c.408C>G NP_000481.2:p.Asp136Glu
XM_011529267.1:c.408C>G XP_011527569.1:p.Asp136Glu
XM_011529267.2:c.408C>G XP_011527569.1:p.Asp136Glu
NM_000490.5:c.408C>G MANE Select NP_000481.2:p.Asp136Glu
Search 100 bp 5'
Search 100 bp 3'