Canonical Allele Identifier: CA344828836
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1284883
ClinVar RCV Id: RCV001700599
dbSNP Id: rs2102713573
MyVariant Identifiers: chr1:g.215901563G>A (hg19) chr1:g.215728221G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215728221G>A , CM000663.2:g.215728221G>A GRCh38
NC_000001.10:g.215901563G>A , CM000663.1:g.215901563G>A GRCh37
NC_000001.9:g.213968186G>A NCBI36
NG_009497.1:g.700176C>T
NG_009497.2:g.700228C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.11875C>T MANE Select ENSP00000305941.3:p.Gln3959Ter
ENST00000674083.1:c.11875C>T ENSP00000501296.1:p.Gln3959Ter
ENST00000307340.7:c.11875C>T ENSP00000305941.3:p.Gln3959Ter
NM_206933.2:c.11875C>T NP_996816.2:p.Gln3959Ter
NM_206933.3:c.11875C>T NP_996816.2:p.Gln3959Ter
NM_206933.4:c.11875C>T MANE Select NP_996816.3:p.Gln3959Ter
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