Canonical Allele Identifier: CA423313769
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1102196
ClinVar RCV Id: RCV001425412
dbSNP Id: rs764453827

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215867029G>T , CM000663.2:g.215867029G>T GRCh38
NC_000001.10:g.216040371G>T , CM000663.1:g.216040371G>T GRCh37
NC_000001.9:g.214106994G>T NCBI36
NG_009497.1:g.561368C>A
NG_009497.2:g.561420C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.8823C>A MANE Select ENSP00000305941.3:p.Ile2941=
ENST00000674083.1:c.8823C>A ENSP00000501296.1:p.Ile2941=
ENST00000307340.7:c.8823C>A ENSP00000305941.3:p.Ile2941=
NM_206933.2:c.8823C>A NP_996816.2:p.Ile2941=
NM_206933.3:c.8823C>A NP_996816.2:p.Ile2941=
NM_206933.4:c.8823C>A MANE Select NP_996816.3:p.Ile2941=