Canonical Allele Identifier: CA37412976
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 797835
ClinVar RCV Id: RCV000981314
dbSNP Id: rs878928366

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215675209C>T , CM000663.2:g.215675209C>T GRCh38
NC_000001.10:g.215848551C>T , CM000663.1:g.215848551C>T GRCh37
NC_000001.9:g.213915174C>T NCBI36
NG_009497.1:g.753188G>A
NG_009497.2:g.753240G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.12702G>A MANE Select ENSP00000305941.3:p.Thr4234=
ENST00000674083.1:c.12702G>A ENSP00000501296.1:p.Thr4234=
ENST00000307340.7:c.12702G>A ENSP00000305941.3:p.Thr4234=
NM_206933.2:c.12702G>A NP_996816.2:p.Thr4234=
NM_206933.3:c.12702G>A NP_996816.2:p.Thr4234=
NM_206933.4:c.12702G>A MANE Select NP_996816.3:p.Thr4234=