Canonical Allele Identifier: CA423428427
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2982511
ClinVar RCV Id: RCV003843158
dbSNP Id: rs1657982987
MyVariant Identifiers: chr1:g.215848635C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215675293C>T , CM000663.2:g.215675293C>T GRCh38
NC_000001.10:g.215848635C>T , CM000663.1:g.215848635C>T GRCh37
NC_000001.9:g.213915258C>T NCBI36
NG_009497.1:g.753104G>A
NG_009497.2:g.753156G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.12618G>A MANE Select ENSP00000305941.3:p.Gln4206=
ENST00000674083.1:c.12618G>A ENSP00000501296.1:p.Gln4206=
ENST00000307340.7:c.12618G>A ENSP00000305941.3:p.Gln4206=
NM_206933.2:c.12618G>A NP_996816.2:p.Gln4206=
NM_206933.3:c.12618G>A NP_996816.2:p.Gln4206=
NM_206933.4:c.12618G>A MANE Select NP_996816.3:p.Gln4206=