Canonical Allele Identifier: CA270788
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 156393
dbSNP Id: rs587783023

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.216246980C>G , CM000663.2:g.216246980C>G GRCh38
NC_000001.10:g.216420322C>G , CM000663.1:g.216420322C>G GRCh37
NC_000001.9:g.214486945C>G NCBI36
NG_009497.1:g.181417G>C
NG_009497.2:g.181469G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000307340.8:c.2414G>C MANE Select ENSP00000305941.3:p.Gly805Ala
ENST00000674083.1:c.2414G>C ENSP00000501296.1:p.Gly805Ala
ENST00000307340.7:c.2414G>C ENSP00000305941.3:p.Gly805Ala
ENST00000366942.3:c.2414G>C ENSP00000355909.3:p.Gly805Ala
NM_007123.5:c.2414G>C NP_009054.5:p.Gly805Ala
NM_206933.2:c.2414G>C NP_996816.2:p.Gly805Ala
NM_206933.3:c.2414G>C NP_996816.2:p.Gly805Ala
NM_007123.6:c.2414G>C NP_009054.6:p.Gly805Ala
NM_206933.4:c.2414G>C MANE Select NP_996816.3:p.Gly805Ala