Canonical Allele Identifier: CA423431427
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2100851
ClinVar RCV Id: RCV003033595
dbSNP Id: rs2036065538
MyVariant Identifiers: chr1:g.216420414T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.216247072T>C , CM000663.2:g.216247072T>C GRCh38
NC_000001.10:g.216420414T>C , CM000663.1:g.216420414T>C GRCh37
NC_000001.9:g.214487037T>C NCBI36
NG_009497.1:g.181325A>G
NG_009497.2:g.181377A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.2322A>G MANE Select ENSP00000305941.3:p.Gly774=
ENST00000674083.1:c.2322A>G ENSP00000501296.1:p.Gly774=
ENST00000307340.7:c.2322A>G ENSP00000305941.3:p.Gly774=
ENST00000366942.3:c.2322A>G ENSP00000355909.3:p.Gly774=
NM_007123.5:c.2322A>G NP_009054.5:p.Gly774=
NM_206933.2:c.2322A>G NP_996816.2:p.Gly774=
NM_206933.3:c.2322A>G NP_996816.2:p.Gly774=
NM_007123.6:c.2322A>G NP_009054.6:p.Gly774=
NM_206933.4:c.2322A>G MANE Select NP_996816.3:p.Gly774=