Canonical Allele Identifier: CA1220426053
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215798980A= , CM000663.2:g.215798980A= GRCh38
NC_000001.10:g.215972322A= , CM000663.1:g.215972322A= GRCh37
NC_000001.9:g.214038945A= NCBI36
NG_009497.1:g.629417T=
NG_009497.2:g.629469T=

Transcript Alleles

HGVS Amino-acid change
ENST00000307340.8:c.9885T= MANE Select ENSP00000305941.3:p.Cys3295=
ENST00000674083.1:c.9885T= ENSP00000501296.1:p.Cys3295=
ENST00000307340.7:c.9885T= ENSP00000305941.3:p.Cys3295=
NM_206933.2:c.9885T= NP_996816.2:p.Cys3295=
NM_206933.3:c.9885T= NP_996816.2:p.Cys3295=
NM_206933.4:c.9885T= MANE Select NP_996816.3:p.Cys3295=