Canonical Allele Identifier: CA384771794
Gene: AQP2 HGNC NCBI

Linked Data

dbSNP Id: rs1947324124
gnomAD v4: 12-49950946-C-A
MyVariant Identifiers: chr12:g.50344729C>A (hg19) chr12:g.49950946C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49950946C>A , CM000674.2:g.49950946C>A GRCh38
NC_000012.11:g.50344729C>A , CM000674.1:g.50344729C>A GRCh37
NC_000012.10:g.48630996C>A NCBI36
NG_008913.1:g.5206C>A , LRG_717:g.5206C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000199280.4:c.116C>A MANE Select ENSP00000199280.3:p.Pro39His
ENST00000199280.3:c.116C>A ENSP00000199280.3:p.Pro39His
ENST00000550862.1:c.116C>A ENSP00000450022.1:p.Pro39His
ENST00000551526.5:c.116C>A ENSP00000447148.1:p.Pro39His
NM_000486.5:c.116C>A , LRG_717t1:c.116C>A NP_000477.1:p.Pro39His
NM_000486.6:c.116C>A MANE Select NP_000477.1:p.Pro39His
Search 100 bp 5'
Search 100 bp 3'