Canonical Allele Identifier: CA344829590
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1909574
ClinVar RCV Id: RCV002587476

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215728334C>T , CM000663.2:g.215728334C>T GRCh38
NC_000001.10:g.215901676C>T , CM000663.1:g.215901676C>T GRCh37
NC_000001.9:g.213968299C>T NCBI36
NG_009497.1:g.700063G>A
NG_009497.2:g.700115G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.11762G>A MANE Select ENSP00000305941.3:p.Gly3921Glu
ENST00000674083.1:c.11762G>A ENSP00000501296.1:p.Gly3921Glu
ENST00000307340.7:c.11762G>A ENSP00000305941.3:p.Gly3921Glu
NM_206933.2:c.11762G>A NP_996816.2:p.Gly3921Glu
NM_206933.3:c.11762G>A NP_996816.2:p.Gly3921Glu
NM_206933.4:c.11762G>A MANE Select NP_996816.3:p.Gly3921Glu