Canonical Allele Identifier: CA423430033
Gene: USH2A HGNC NCBI

Linked Data

dbSNP Id: rs779184532
MyVariant Identifiers: chr1:g.215901525A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215728183A>T , CM000663.2:g.215728183A>T GRCh38
NC_000001.10:g.215901525A>T , CM000663.1:g.215901525A>T GRCh37
NC_000001.9:g.213968148A>T NCBI36
NG_009497.1:g.700214T>A
NG_009497.2:g.700266T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.11913T>A MANE Select ENSP00000305941.3:p.Pro3971=
ENST00000674083.1:c.11913T>A ENSP00000501296.1:p.Pro3971=
ENST00000307340.7:c.11913T>A ENSP00000305941.3:p.Pro3971=
NM_206933.2:c.11913T>A NP_996816.2:p.Pro3971=
NM_206933.3:c.11913T>A NP_996816.2:p.Pro3971=
NM_206933.4:c.11913T>A MANE Select NP_996816.3:p.Pro3971=