Canonical Allele Identifier: CA262067
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 48369
dbSNP Id: rs111033382

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215759659C>A , CM000663.2:g.215759659C>A GRCh38
NC_000001.10:g.215933001C>A , CM000663.1:g.215933001C>A GRCh37
NC_000001.9:g.213999624C>A NCBI36
NG_009497.1:g.668738G>T
NG_009497.2:g.668790G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.11231+1G>T MANE Select ENSP00000305941.3:n.11231+1G>T
ENST00000674083.1:c.11231+1G>T ENSP00000501296.1:n.11231+1G>T
ENST00000307340.7:c.11231+1G>T ENSP00000305941.3:n.11231+1G>T
NM_206933.2:c.11231+1G>T NP_996816.2:n.11231+1G>T
NM_206933.3:c.11231+1G>T NP_996816.2:n.11231+1G>T
NM_206933.4:c.11231+1G>T MANE Select NP_996816.3:n.11231+1G>T