Canonical Allele Identifier: CA6559165
Gene: AQP2 HGNC NCBI

Linked Data

dbSNP Id: rs544999593
ExAC: 12:50344806 G / A
gnomAD v2: 12-50344806-G-A
gnomAD v3: 12-49951023-G-A
gnomAD v4: 12-49951023-G-A
MyVariant Identifiers: chr12:g.50344806G>A (hg19) chr12:g.49951023G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49951023G>A , CM000674.2:g.49951023G>A GRCh38
NC_000012.11:g.50344806G>A , CM000674.1:g.50344806G>A GRCh37
NC_000012.10:g.48631073G>A NCBI36
NG_008913.1:g.5283G>A , LRG_717:g.5283G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000199280.4:c.193G>A MANE Select ENSP00000199280.3:p.Ala65Thr
ENST00000199280.3:c.193G>A ENSP00000199280.3:p.Ala65Thr
ENST00000550862.1:c.193G>A ENSP00000450022.1:p.Ala65Thr
ENST00000551526.5:c.193G>A ENSP00000447148.1:p.Ala65Thr
NM_000486.5:c.193G>A , LRG_717t1:c.193G>A NP_000477.1:p.Ala65Thr
NM_000486.6:c.193G>A MANE Select NP_000477.1:p.Ala65Thr
Search 100 bp 5'
Search 100 bp 3'