Canonical Allele Identifier: CA1394502
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1094772
ClinVar RCV Id: RCV001415437
dbSNP Id: rs756401705

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215867053C>T , CM000663.2:g.215867053C>T GRCh38
NC_000001.10:g.216040395C>T , CM000663.1:g.216040395C>T GRCh37
NC_000001.9:g.214107018C>T NCBI36
NG_009497.1:g.561344G>A
NG_009497.2:g.561396G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.8799G>A MANE Select ENSP00000305941.3:p.Ala2933=
ENST00000674083.1:c.8799G>A ENSP00000501296.1:p.Ala2933=
ENST00000307340.7:c.8799G>A ENSP00000305941.3:p.Ala2933=
NM_206933.2:c.8799G>A NP_996816.2:p.Ala2933=
NM_206933.3:c.8799G>A NP_996816.2:p.Ala2933=
NM_206933.4:c.8799G>A MANE Select NP_996816.3:p.Ala2933=