Canonical Allele Identifier: CA731376841
Gene: USH2A HGNC NCBI

Linked Data

dbSNP Id: rs1176415827
gnomAD v3: 1-215845732-A-C
gnomAD v4: 1-215845732-A-C
MyVariant Identifiers: chr1:g.216019074A>C (hg19) chr1:g.215845732A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215845732A>C , CM000663.2:g.215845732A>C GRCh38
NC_000001.10:g.216019074A>C , CM000663.1:g.216019074A>C GRCh37
NC_000001.9:g.214085697A>C NCBI36
NG_009497.1:g.582665T>G
NG_009497.2:g.582717T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000307340.8:c.9055+92T>G MANE Select ENSP00000305941.3:n.9055+92T>G
ENST00000674083.1:c.9055+92T>G ENSP00000501296.1:n.9055+92T>G
ENST00000307340.7:c.9055+92T>G ENSP00000305941.3:n.9055+92T>G
NM_206933.2:c.9055+92T>G NP_996816.2:n.9055+92T>G
NM_206933.3:c.9055+92T>G NP_996816.2:n.9055+92T>G
NM_206933.4:c.9055+92T>G MANE Select NP_996816.3:n.9055+92T>G
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