Canonical Allele Identifier: CA16043856
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 374703
ClinVar RCV Id: RCV000416258
dbSNP Id: rs1057519208
MyVariant Identifiers: chr1:g.216019173G>T (hg19) chr1:g.215845831G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215845831G>T , CM000663.2:g.215845831G>T GRCh38
NC_000001.10:g.216019173G>T , CM000663.1:g.216019173G>T GRCh37
NC_000001.9:g.214085796G>T NCBI36
NG_009497.1:g.582566C>A
NG_009497.2:g.582618C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000307340.8:c.9048C>A MANE Select ENSP00000305941.3:p.Cys3016Ter
ENST00000674083.1:c.9048C>A ENSP00000501296.1:p.Cys3016Ter
ENST00000307340.7:c.9048C>A ENSP00000305941.3:p.Cys3016Ter
NM_206933.2:c.9048C>A NP_996816.2:p.Cys3016Ter
NM_206933.3:c.9048C>A NP_996816.2:p.Cys3016Ter
NM_206933.4:c.9048C>A MANE Select NP_996816.3:p.Cys3016Ter
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