Canonical Allele Identifier: CA423430114
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1652966
ClinVar RCV Id: RCV002158649
dbSNP Id: rs2102713730
MyVariant Identifiers: chr1:g.215901645G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215728303G>A , CM000663.2:g.215728303G>A GRCh38
NC_000001.10:g.215901645G>A , CM000663.1:g.215901645G>A GRCh37
NC_000001.9:g.213968268G>A NCBI36
NG_009497.1:g.700094C>T
NG_009497.2:g.700146C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.11793C>T MANE Select ENSP00000305941.3:p.Thr3931=
ENST00000674083.1:c.11793C>T ENSP00000501296.1:p.Thr3931=
ENST00000307340.7:c.11793C>T ENSP00000305941.3:p.Thr3931=
NM_206933.2:c.11793C>T NP_996816.2:p.Thr3931=
NM_206933.3:c.11793C>T NP_996816.2:p.Thr3931=
NM_206933.4:c.11793C>T MANE Select NP_996816.3:p.Thr3931=