Canonical Allele Identifier: CA344845369
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 844877
ClinVar RCV Id: RCV001047836
dbSNP Id: rs1657932622
MyVariant Identifiers: chr1:g.215847846G>T (hg19) chr1:g.215674504G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215674504G>T , CM000663.2:g.215674504G>T GRCh38
NC_000001.10:g.215847846G>T , CM000663.1:g.215847846G>T GRCh37
NC_000001.9:g.213914469G>T NCBI36
NG_009497.1:g.753893C>A
NG_009497.2:g.753945C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.13407C>A MANE Select ENSP00000305941.3:p.Asn4469Lys
ENST00000674083.1:c.13407C>A ENSP00000501296.1:p.Asn4469Lys
ENST00000307340.7:c.13407C>A ENSP00000305941.3:p.Asn4469Lys
NM_206933.2:c.13407C>A NP_996816.2:p.Asn4469Lys
NM_206933.3:c.13407C>A NP_996816.2:p.Asn4469Lys
NM_206933.4:c.13407C>A MANE Select NP_996816.3:p.Asn4469Lys
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