Canonical Allele Identifier: CA2650528726
Gene: USH2A HGNC NCBI

Linked Data

gnomAD v4: 1-215845746-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215845746A>T , CM000663.2:g.215845746A>T GRCh38
NC_000001.10:g.216019088A>T , CM000663.1:g.216019088A>T GRCh37
NC_000001.9:g.214085711A>T NCBI36
NG_009497.1:g.582651T>A
NG_009497.2:g.582703T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.9055+78T>A MANE Select ENSP00000305941.3:n.9055+78T>A
ENST00000674083.1:c.9055+78T>A ENSP00000501296.1:n.9055+78T>A
ENST00000307340.7:c.9055+78T>A ENSP00000305941.3:n.9055+78T>A
NM_206933.2:c.9055+78T>A NP_996816.2:n.9055+78T>A
NM_206933.3:c.9055+78T>A NP_996816.2:n.9055+78T>A
NM_206933.4:c.9055+78T>A MANE Select NP_996816.3:n.9055+78T>A
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