Canonical Allele Identifier: CA37435993
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1204391
ClinVar RCV Id: RCV001570726
dbSNP Id: rs7514451
gnomAD v2: 1-215953480-C-T
gnomAD v3: 1-215780138-C-T
gnomAD v4: 1-215780138-C-T
MyVariant Identifiers: chr1:g.215953480C>T (hg19) chr1:g.215780138C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215780138C>T , CM000663.2:g.215780138C>T GRCh38
NC_000001.10:g.215953480C>T , CM000663.1:g.215953480C>T GRCh37
NC_000001.9:g.214020103C>T NCBI36
NG_009497.1:g.648259G>A
NG_009497.2:g.648311G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.10741-97G>A MANE Select ENSP00000305941.3:n.10741-97G>A
ENST00000674083.1:c.10741-97G>A ENSP00000501296.1:n.10741-97G>A
ENST00000307340.7:c.10741-97G>A ENSP00000305941.3:n.10741-97G>A
NM_206933.2:c.10741-97G>A NP_996816.2:n.10741-97G>A
NM_206933.3:c.10741-97G>A NP_996816.2:n.10741-97G>A
NM_206933.4:c.10741-97G>A MANE Select NP_996816.3:n.10741-97G>A
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