Canonical Allele Identifier: CA344850717
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 856772
ClinVar RCV Id: RCV001062307
dbSNP Id: rs1657987278

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215675386C>A , CM000663.2:g.215675386C>A GRCh38
NC_000001.10:g.215848728C>A , CM000663.1:g.215848728C>A GRCh37
NC_000001.9:g.213915351C>A NCBI36
NG_009497.1:g.753011G>T
NG_009497.2:g.753063G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.12525G>T MANE Select ENSP00000305941.3:p.Trp4175Cys
ENST00000674083.1:c.12525G>T ENSP00000501296.1:p.Trp4175Cys
ENST00000307340.7:c.12525G>T ENSP00000305941.3:p.Trp4175Cys
NM_206933.2:c.12525G>T NP_996816.2:p.Trp4175Cys
NM_206933.3:c.12525G>T NP_996816.2:p.Trp4175Cys
NM_206933.4:c.12525G>T MANE Select NP_996816.3:p.Trp4175Cys