Canonical Allele Identifier: CA9739501
Gene: AVP HGNC NCBI

Linked Data

dbSNP Id: rs556025430
gnomAD v2: 20-3065268-G-C
gnomAD v3: 20-3084622-G-C
gnomAD v4: 20-3084622-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3084622G>C , CM000682.2:g.3084622G>C GRCh38
NC_000020.10:g.3065268G>C , CM000682.1:g.3065268G>C GRCh37
NC_000020.9:g.3013268G>C NCBI36
NG_008663.1:g.5103C>G , LRG_715:g.5103C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000380293.3:c.53C>G MANE Select ENSP00000369647.3:p.Ser18Cys
NM_000490.4:c.53C>G , LRG_715t1:c.53C>G NP_000481.2:p.Ser18Cys
XM_011529267.1:c.53C>G XP_011527569.1:p.Ser18Cys
XM_011529267.2:c.53C>G XP_011527569.1:p.Ser18Cys
NM_000490.5:c.53C>G MANE Select NP_000481.2:p.Ser18Cys