Canonical Allele Identifier: CA423313987
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2866833
ClinVar RCV Id: RCV003700420
dbSNP Id: rs1470396110

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215867152A>G , CM000663.2:g.215867152A>G GRCh38
NC_000001.10:g.216040494A>G , CM000663.1:g.216040494A>G GRCh37
NC_000001.9:g.214107117A>G NCBI36
NG_009497.1:g.561245T>C
NG_009497.2:g.561297T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.8700T>C MANE Select ENSP00000305941.3:p.Tyr2900=
ENST00000674083.1:c.8700T>C ENSP00000501296.1:p.Tyr2900=
ENST00000307340.7:c.8700T>C ENSP00000305941.3:p.Tyr2900=
NM_206933.2:c.8700T>C NP_996816.2:p.Tyr2900=
NM_206933.3:c.8700T>C NP_996816.2:p.Tyr2900=
NM_206933.4:c.8700T>C MANE Select NP_996816.3:p.Tyr2900=