Canonical Allele Identifier: CA423312050
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1538049
ClinVar RCV Id: RCV002159642
dbSNP Id: rs1346542375

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215675614T>C , CM000663.2:g.215675614T>C GRCh38
NC_000001.10:g.215848956T>C , CM000663.1:g.215848956T>C GRCh37
NC_000001.9:g.213915579T>C NCBI36
NG_009497.1:g.752783A>G
NG_009497.2:g.752835A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.12297A>G MANE Select ENSP00000305941.3:p.Thr4099=
ENST00000674083.1:c.12297A>G ENSP00000501296.1:p.Thr4099=
ENST00000307340.7:c.12297A>G ENSP00000305941.3:p.Thr4099=
NM_206933.2:c.12297A>G NP_996816.2:p.Thr4099=
NM_206933.3:c.12297A>G NP_996816.2:p.Thr4099=
NM_206933.4:c.12297A>G MANE Select NP_996816.3:p.Thr4099=