Canonical Allele Identifier: CA1141863988
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215728169G= , CM000663.2:g.215728169G= GRCh38
NC_000001.10:g.215901511G= , CM000663.1:g.215901511G= GRCh37
NC_000001.9:g.213968134G= NCBI36
NG_009497.1:g.700228C=
NG_009497.2:g.700280C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.11927C= MANE Select ENSP00000305941.3:p.Thr3976=
ENST00000674083.1:c.11927C= ENSP00000501296.1:p.Thr3976=
ENST00000307340.7:c.11927C= ENSP00000305941.3:p.Thr3976=
NM_206933.2:c.11927C= NP_996816.2:p.Thr3976=
NM_206933.3:c.11927C= NP_996816.2:p.Thr3976=
NM_206933.4:c.11927C= MANE Select NP_996816.3:p.Thr3976=