Canonical Allele Identifier: CA344836370
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 444199
ClinVar RCV Id: RCV000512654
dbSNP Id: rs1553261365
MyVariant Identifiers: chr1:g.215955431A>G (hg19) chr1:g.215782089A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215782089A>G , CM000663.2:g.215782089A>G GRCh38
NC_000001.10:g.215955431A>G , CM000663.1:g.215955431A>G GRCh37
NC_000001.9:g.214022054A>G NCBI36
NG_009497.1:g.646308T>C
NG_009497.2:g.646360T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000307340.8:c.10693T>C MANE Select ENSP00000305941.3:p.Tyr3565His
ENST00000674083.1:c.10693T>C ENSP00000501296.1:p.Tyr3565His
ENST00000307340.7:c.10693T>C ENSP00000305941.3:p.Tyr3565His
NM_206933.2:c.10693T>C NP_996816.2:p.Tyr3565His
NM_206933.3:c.10693T>C NP_996816.2:p.Tyr3565His
NM_206933.4:c.10693T>C MANE Select NP_996816.3:p.Tyr3565His
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