Canonical Allele Identifier: CA1220396589
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215728370A= , CM000663.2:g.215728370A= GRCh38
NC_000001.10:g.215901712A= , CM000663.1:g.215901712A= GRCh37
NC_000001.9:g.213968335A= NCBI36
NG_009497.1:g.700027T=
NG_009497.2:g.700079T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.11726T= MANE Select ENSP00000305941.3:p.Ile3909=
ENST00000674083.1:c.11726T= ENSP00000501296.1:p.Ile3909=
ENST00000307340.7:c.11726T= ENSP00000305941.3:p.Ile3909=
NM_206933.2:c.11726T= NP_996816.2:p.Ile3909=
NM_206933.3:c.11726T= NP_996816.2:p.Ile3909=
NM_206933.4:c.11726T= MANE Select NP_996816.3:p.Ile3909=