Canonical Allele Identifier: CA6559177
Gene: AQP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1455736
ClinVar RCV Id: RCV001970106
dbSNP Id: rs781478659
ExAC: 12:50344866 C / T
gnomAD v2: 12-50344866-C-T
gnomAD v4: 12-49951083-C-T
COSMIC: COSM3461773
MyVariant Identifiers: chr12:g.50344866C>T (hg19) chr12:g.49951083C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49951083C>T , CM000674.2:g.49951083C>T GRCh38
NC_000012.11:g.50344866C>T , CM000674.1:g.50344866C>T GRCh37
NC_000012.10:g.48631133C>T NCBI36
NG_008913.1:g.5343C>T , LRG_717:g.5343C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000199280.4:c.253C>T MANE Select ENSP00000199280.3:p.Arg85Ter
ENST00000199280.3:c.253C>T ENSP00000199280.3:p.Arg85Ter
ENST00000550862.1:c.253C>T ENSP00000450022.1:p.Arg85Ter
ENST00000551526.5:c.253C>T ENSP00000447148.1:p.Arg85Ter
NM_000486.5:c.253C>T , LRG_717t1:c.253C>T NP_000477.1:p.Arg85Ter
NM_000486.6:c.253C>T MANE Select NP_000477.1:p.Arg85Ter
Search 100 bp 5'
Search 100 bp 3'