Canonical Allele Identifier: CA143277
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 48386
dbSNP Id: rs55961436

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215728168C>T , CM000663.2:g.215728168C>T GRCh38
NC_000001.10:g.215901510C>T , CM000663.1:g.215901510C>T GRCh37
NC_000001.9:g.213968133C>T NCBI36
NG_009497.1:g.700229G>A
NG_009497.2:g.700281G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.11928G>A MANE Select ENSP00000305941.3:p.Thr3976=
ENST00000674083.1:c.11928G>A ENSP00000501296.1:p.Thr3976=
ENST00000307340.7:c.11928G>A ENSP00000305941.3:p.Thr3976=
NM_206933.2:c.11928G>A NP_996816.2:p.Thr3976=
NM_206933.3:c.11928G>A NP_996816.2:p.Thr3976=
NM_206933.4:c.11928G>A MANE Select NP_996816.3:p.Thr3976=