Canonical Allele Identifier: CA1220413084
Gene: USH2A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215767050C= , CM000663.2:g.215767050C= GRCh38
NC_000001.10:g.215940392C= , CM000663.1:g.215940392C= GRCh37
NC_000001.9:g.214007015C= NCBI36
NG_009497.1:g.661347G=
NG_009497.2:g.661399G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.10940-262G= MANE Select ENSP00000305941.3:n.10940-262G=
ENST00000674083.1:c.10940-262G= ENSP00000501296.1:n.10940-262G=
ENST00000307340.7:c.10940-262G= ENSP00000305941.3:n.10940-262G=
NM_206933.2:c.10940-262G= NP_996816.2:n.10940-262G=
NM_206933.3:c.10940-262G= NP_996816.2:n.10940-262G=
NM_206933.4:c.10940-262G= MANE Select NP_996816.3:n.10940-262G=
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