Canonical Allele Identifier: CA1141674471
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215867128C= , CM000663.2:g.215867128C= GRCh38
NC_000001.10:g.216040470C= , CM000663.1:g.216040470C= GRCh37
NC_000001.9:g.214107093C= NCBI36
NG_009497.1:g.561269G=
NG_009497.2:g.561321G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.8724G= MANE Select ENSP00000305941.3:p.Val2908=
ENST00000674083.1:c.8724G= ENSP00000501296.1:p.Val2908=
ENST00000307340.7:c.8724G= ENSP00000305941.3:p.Val2908=
NM_206933.2:c.8724G= NP_996816.2:p.Val2908=
NM_206933.3:c.8724G= NP_996816.2:p.Val2908=
NM_206933.4:c.8724G= MANE Select NP_996816.3:p.Val2908=