Canonical Allele Identifier: CA1393477
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1140790
ClinVar RCV Id: RCV001477983
dbSNP Id: rs749359912

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215675524T>A , CM000663.2:g.215675524T>A GRCh38
NC_000001.10:g.215848866T>A , CM000663.1:g.215848866T>A GRCh37
NC_000001.9:g.213915489T>A NCBI36
NG_009497.1:g.752873A>T
NG_009497.2:g.752925A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.12387A>T MANE Select ENSP00000305941.3:p.Thr4129=
ENST00000674083.1:c.12387A>T ENSP00000501296.1:p.Thr4129=
ENST00000307340.7:c.12387A>T ENSP00000305941.3:p.Thr4129=
NM_206933.2:c.12387A>T NP_996816.2:p.Thr4129=
NM_206933.3:c.12387A>T NP_996816.2:p.Thr4129=
NM_206933.4:c.12387A>T MANE Select NP_996816.3:p.Thr4129=