Canonical Allele Identifier: CA2739275654
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2901080
ClinVar RCV Id: RCV003731114
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.216247238A>G , CM000663.2:g.216247238A>G GRCh38
NC_000001.10:g.216420580A>G , CM000663.1:g.216420580A>G GRCh37
NC_000001.9:g.214487203A>G NCBI36
NG_009497.1:g.181159T>C
NG_009497.2:g.181211T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.2168-12T>C MANE Select ENSP00000305941.3:n.2168-12T>C
ENST00000674083.1:c.2168-12T>C ENSP00000501296.1:n.2168-12T>C
ENST00000307340.7:c.2168-12T>C ENSP00000305941.3:n.2168-12T>C
ENST00000366942.3:c.2168-12T>C ENSP00000355909.3:n.2168-12T>C
NM_007123.5:c.2168-12T>C NP_009054.5:n.2168-12T>C
NM_206933.2:c.2168-12T>C NP_996816.2:n.2168-12T>C
NM_206933.3:c.2168-12T>C NP_996816.2:n.2168-12T>C
NM_007123.6:c.2168-12T>C NP_009054.6:n.2168-12T>C
NM_206933.4:c.2168-12T>C MANE Select NP_996816.3:n.2168-12T>C
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