Canonical Allele Identifier: CA1148280323
Gene: USH2A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215816966A= , CM000663.2:g.215816966A= GRCh38
NC_000001.10:g.215990308A= , CM000663.1:g.215990308A= GRCh37
NC_000001.9:g.214056931A= NCBI36
NG_009497.1:g.611431T=
NG_009497.2:g.611483T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.9570+31T= MANE Select ENSP00000305941.3:n.9570+31T=
ENST00000674083.1:c.9570+31T= ENSP00000501296.1:n.9570+31T=
ENST00000307340.7:c.9570+31T= ENSP00000305941.3:n.9570+31T=
NM_206933.2:c.9570+31T= NP_996816.2:n.9570+31T=
NM_206933.3:c.9570+31T= NP_996816.2:n.9570+31T=
NM_206933.4:c.9570+31T= MANE Select NP_996816.3:n.9570+31T=
Search 100 bp 5'
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