Canonical Allele Identifier: CA423313761
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1100471
ClinVar RCV Id: RCV001423099
dbSNP Id: rs1422830491

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215867022T>G , CM000663.2:g.215867022T>G GRCh38
NC_000001.10:g.216040364T>G , CM000663.1:g.216040364T>G GRCh37
NC_000001.9:g.214106987T>G NCBI36
NG_009497.1:g.561375A>C
NG_009497.2:g.561427A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.8830A>C MANE Select ENSP00000305941.3:p.Arg2944=
ENST00000674083.1:c.8830A>C ENSP00000501296.1:p.Arg2944=
ENST00000307340.7:c.8830A>C ENSP00000305941.3:p.Arg2944=
NM_206933.2:c.8830A>C NP_996816.2:p.Arg2944=
NM_206933.3:c.8830A>C NP_996816.2:p.Arg2944=
NM_206933.4:c.8830A>C MANE Select NP_996816.3:p.Arg2944=