Canonical Allele Identifier: CA1147659175
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215675156G= , CM000663.2:g.215675156G= GRCh38
NC_000001.10:g.215848498G= , CM000663.1:g.215848498G= GRCh37
NC_000001.9:g.213915121G= NCBI36
NG_009497.1:g.753241C=
NG_009497.2:g.753293C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.12755C= MANE Select ENSP00000305941.3:p.Ser4252=
ENST00000674083.1:c.12755C= ENSP00000501296.1:p.Ser4252=
ENST00000307340.7:c.12755C= ENSP00000305941.3:p.Ser4252=
NM_206933.2:c.12755C= NP_996816.2:p.Ser4252=
NM_206933.3:c.12755C= NP_996816.2:p.Ser4252=
NM_206933.4:c.12755C= MANE Select NP_996816.3:p.Ser4252=