Canonical Allele Identifier: CA37410113
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 557599
dbSNP Id: rs1040917329

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215671088A>G , CM000663.2:g.215671088A>G GRCh38
NC_000001.10:g.215844430A>G , CM000663.1:g.215844430A>G GRCh37
NC_000001.9:g.213911053A>G NCBI36
NG_009497.1:g.757309T>C
NG_009497.2:g.757361T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.14017T>C MANE Select ENSP00000305941.3:p.Tyr4673His
ENST00000674083.1:c.14017T>C ENSP00000501296.1:p.Tyr4673His
ENST00000307340.7:c.14017T>C ENSP00000305941.3:p.Tyr4673His
NM_206933.2:c.14017T>C NP_996816.2:p.Tyr4673His
NM_206933.3:c.14017T>C NP_996816.2:p.Tyr4673His
NM_206933.4:c.14017T>C MANE Select NP_996816.3:p.Tyr4673His