Canonical Allele Identifier: CA1394532
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1153327
ClinVar RCV Id: RCV001494975
dbSNP Id: rs774764404

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215867140T>C , CM000663.2:g.215867140T>C GRCh38
NC_000001.10:g.216040482T>C , CM000663.1:g.216040482T>C GRCh37
NC_000001.9:g.214107105T>C NCBI36
NG_009497.1:g.561257A>G
NG_009497.2:g.561309A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.8712A>G MANE Select ENSP00000305941.3:p.Val2904=
ENST00000674083.1:c.8712A>G ENSP00000501296.1:p.Val2904=
ENST00000307340.7:c.8712A>G ENSP00000305941.3:p.Val2904=
NM_206933.2:c.8712A>G NP_996816.2:p.Val2904=
NM_206933.3:c.8712A>G NP_996816.2:p.Val2904=
NM_206933.4:c.8712A>G MANE Select NP_996816.3:p.Val2904=