Canonical Allele Identifier: CA143607
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 48589
dbSNP Id: rs56385601

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215888964A>G , CM000663.2:g.215888964A>G GRCh38
NC_000001.10:g.216062306A>G , CM000663.1:g.216062306A>G GRCh37
NC_000001.9:g.214128929A>G NCBI36
NG_009497.1:g.539433T>C
NG_009497.2:g.539485T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.7685T>C MANE Select ENSP00000305941.3:p.Val2562Ala
ENST00000674083.1:c.7685T>C ENSP00000501296.1:p.Val2562Ala
ENST00000307340.7:c.7685T>C ENSP00000305941.3:p.Val2562Ala
NM_206933.2:c.7685T>C NP_996816.2:p.Val2562Ala
NM_206933.3:c.7685T>C NP_996816.2:p.Val2562Ala
NM_206933.4:c.7685T>C MANE Select NP_996816.3:p.Val2562Ala