Canonical Allele Identifier: CA384771771
Gene: AQP2 HGNC NCBI

Linked Data

dbSNP Id: rs1947324056

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49950939G>T , CM000674.2:g.49950939G>T GRCh38
NC_000012.11:g.50344722G>T , CM000674.1:g.50344722G>T GRCh37
NC_000012.10:g.48630989G>T NCBI36
NG_008913.1:g.5199G>T , LRG_717:g.5199G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000199280.4:c.109G>T MANE Select ENSP00000199280.3:p.Ala37Ser
ENST00000199280.3:c.109G>T ENSP00000199280.3:p.Ala37Ser
ENST00000550862.1:c.109G>T ENSP00000450022.1:p.Ala37Ser
ENST00000551526.5:c.109G>T ENSP00000447148.1:p.Ala37Ser
NM_000486.5:c.109G>T , LRG_717t1:c.109G>T NP_000477.1:p.Ala37Ser
NM_000486.6:c.109G>T MANE Select NP_000477.1:p.Ala37Ser