Canonical Allele Identifier: CA6559146
Gene: AQP2 HGNC NCBI

Linked Data

dbSNP Id: rs746338782
ExAC: 12:50344716 C / A
gnomAD v2: 12-50344716-C-A
MyVariant Identifiers: chr12:g.50344716C>A (hg19) chr12:g.49950933C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49950933C>A , CM000674.2:g.49950933C>A GRCh38
NC_000012.11:g.50344716C>A , CM000674.1:g.50344716C>A GRCh37
NC_000012.10:g.48630983C>A NCBI36
NG_008913.1:g.5193C>A , LRG_717:g.5193C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000199280.4:c.103C>A MANE Select ENSP00000199280.3:p.Pro35Thr
ENST00000199280.3:c.103C>A ENSP00000199280.3:p.Pro35Thr
ENST00000550862.1:c.103C>A ENSP00000450022.1:p.Pro35Thr
ENST00000551526.5:c.103C>A ENSP00000447148.1:p.Pro35Thr
NM_000486.5:c.103C>A , LRG_717t1:c.103C>A NP_000477.1:p.Pro35Thr
NM_000486.6:c.103C>A MANE Select NP_000477.1:p.Pro35Thr
Search 100 bp 5'
Search 100 bp 3'