Canonical Allele Identifier: CA384772072
Gene: AQP2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.50344799A>G (hg19) chr12:g.49951016A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49951016A>G , CM000674.2:g.49951016A>G GRCh38
NC_000012.11:g.50344799A>G , CM000674.1:g.50344799A>G GRCh37
NC_000012.10:g.48631066A>G NCBI36
NG_008913.1:g.5276A>G , LRG_717:g.5276A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000199280.4:c.186A>G MANE Select ENSP00000199280.3:p.Ile62Met
ENST00000199280.3:c.186A>G ENSP00000199280.3:p.Ile62Met
ENST00000550862.1:c.186A>G ENSP00000450022.1:p.Ile62Met
ENST00000551526.5:c.186A>G ENSP00000447148.1:p.Ile62Met
NM_000486.5:c.186A>G , LRG_717t1:c.186A>G NP_000477.1:p.Ile62Met
NM_000486.6:c.186A>G MANE Select NP_000477.1:p.Ile62Met
Search 100 bp 5'
Search 100 bp 3'