Canonical Allele Identifier: CA262060
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 48355
dbSNP Id: rs202175091

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215782070G>A , CM000663.2:g.215782070G>A GRCh38
NC_000001.10:g.215955412G>A , CM000663.1:g.215955412G>A GRCh37
NC_000001.9:g.214022035G>A NCBI36
NG_009497.1:g.646327C>T
NG_009497.2:g.646379C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000307340.8:c.10712C>T MANE Select ENSP00000305941.3:p.Thr3571Met
ENST00000674083.1:c.10712C>T ENSP00000501296.1:p.Thr3571Met
ENST00000307340.7:c.10712C>T ENSP00000305941.3:p.Thr3571Met
NM_206933.2:c.10712C>T NP_996816.2:p.Thr3571Met
NM_206933.3:c.10712C>T NP_996816.2:p.Thr3571Met
NM_206933.4:c.10712C>T MANE Select NP_996816.3:p.Thr3571Met