Canonical Allele Identifier: CA1396266
Gene: USH2A HGNC NCBI

Linked Data

dbSNP Id: rs777541838

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.216247190A>C , CM000663.2:g.216247190A>C GRCh38
NC_000001.10:g.216420532A>C , CM000663.1:g.216420532A>C GRCh37
NC_000001.9:g.214487155A>C NCBI36
NG_009497.1:g.181207T>G
NG_009497.2:g.181259T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.2204T>G MANE Select ENSP00000305941.3:p.Phe735Cys
ENST00000674083.1:c.2204T>G ENSP00000501296.1:p.Phe735Cys
ENST00000307340.7:c.2204T>G ENSP00000305941.3:p.Phe735Cys
ENST00000366942.3:c.2204T>G ENSP00000355909.3:p.Phe735Cys
NM_007123.5:c.2204T>G NP_009054.5:p.Phe735Cys
NM_206933.2:c.2204T>G NP_996816.2:p.Phe735Cys
NM_206933.3:c.2204T>G NP_996816.2:p.Phe735Cys
NM_007123.6:c.2204T>G NP_009054.6:p.Phe735Cys
NM_206933.4:c.2204T>G MANE Select NP_996816.3:p.Phe735Cys