Canonical Allele Identifier: CA6559173
Gene: AQP2 HGNC NCBI

Linked Data

dbSNP Id: rs763156762
ExAC: 12:50344854 G / A
gnomAD v2: 12-50344854-G-A
gnomAD v3: 12-49951071-G-A
gnomAD v4: 12-49951071-G-A
COSMIC: COSM4042558
MyVariant Identifiers: chr12:g.50344854G>A (hg19) chr12:g.49951071G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49951071G>A , CM000674.2:g.49951071G>A GRCh38
NC_000012.11:g.50344854G>A , CM000674.1:g.50344854G>A GRCh37
NC_000012.10:g.48631121G>A NCBI36
NG_008913.1:g.5331G>A , LRG_717:g.5331G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000199280.4:c.241G>A MANE Select ENSP00000199280.3:p.Val81Ile
ENST00000199280.3:c.241G>A ENSP00000199280.3:p.Val81Ile
ENST00000550862.1:c.241G>A ENSP00000450022.1:p.Val81Ile
ENST00000551526.5:c.241G>A ENSP00000447148.1:p.Val81Ile
NM_000486.5:c.241G>A , LRG_717t1:c.241G>A NP_000477.1:p.Val81Ile
NM_000486.6:c.241G>A MANE Select NP_000477.1:p.Val81Ile
Search 100 bp 5'
Search 100 bp 3'