Canonical Allele Identifier: CA423428050
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2052446
ClinVar RCV Id: RCV002932742
MyVariant Identifiers: chr1:g.215848545A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215675203A>G , CM000663.2:g.215675203A>G GRCh38
NC_000001.10:g.215848545A>G , CM000663.1:g.215848545A>G GRCh37
NC_000001.9:g.213915168A>G NCBI36
NG_009497.1:g.753194T>C
NG_009497.2:g.753246T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.12708T>C MANE Select ENSP00000305941.3:p.Cys4236=
ENST00000674083.1:c.12708T>C ENSP00000501296.1:p.Cys4236=
ENST00000307340.7:c.12708T>C ENSP00000305941.3:p.Cys4236=
NM_206933.2:c.12708T>C NP_996816.2:p.Cys4236=
NM_206933.3:c.12708T>C NP_996816.2:p.Cys4236=
NM_206933.4:c.12708T>C MANE Select NP_996816.3:p.Cys4236=