Canonical Allele Identifier: CA1148334050
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215675415C= , CM000663.2:g.215675415C= GRCh38
NC_000001.10:g.215848757C= , CM000663.1:g.215848757C= GRCh37
NC_000001.9:g.213915380C= NCBI36
NG_009497.1:g.752982G=
NG_009497.2:g.753034G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.12496G= MANE Select ENSP00000305941.3:p.Val4166=
ENST00000674083.1:c.12496G= ENSP00000501296.1:p.Val4166=
ENST00000307340.7:c.12496G= ENSP00000305941.3:p.Val4166=
NM_206933.2:c.12496G= NP_996816.2:p.Val4166=
NM_206933.3:c.12496G= NP_996816.2:p.Val4166=
NM_206933.4:c.12496G= MANE Select NP_996816.3:p.Val4166=