Canonical Allele Identifier: CA1012197680
Gene: USH2A HGNC NCBI

Linked Data

dbSNP Id: rs1662872898
gnomAD v3: 1-215816914-A-G
gnomAD v4: 1-215816914-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215816914A>G , CM000663.2:g.215816914A>G GRCh38
NC_000001.10:g.215990256A>G , CM000663.1:g.215990256A>G GRCh37
NC_000001.9:g.214056879A>G NCBI36
NG_009497.1:g.611483T>C
NG_009497.2:g.611535T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.9570+83T>C MANE Select ENSP00000305941.3:n.9570+83T>C
ENST00000674083.1:c.9570+83T>C ENSP00000501296.1:n.9570+83T>C
ENST00000307340.7:c.9570+83T>C ENSP00000305941.3:n.9570+83T>C
NM_206933.2:c.9570+83T>C NP_996816.2:n.9570+83T>C
NM_206933.3:c.9570+83T>C NP_996816.2:n.9570+83T>C
NM_206933.4:c.9570+83T>C MANE Select NP_996816.3:n.9570+83T>C
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