Canonical Allele Identifier: CA423430129
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1127084
ClinVar RCV Id: RCV001459347
dbSNP Id: rs2102713763
MyVariant Identifiers: chr1:g.215901672G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215728330G>T , CM000663.2:g.215728330G>T GRCh38
NC_000001.10:g.215901672G>T , CM000663.1:g.215901672G>T GRCh37
NC_000001.9:g.213968295G>T NCBI36
NG_009497.1:g.700067C>A
NG_009497.2:g.700119C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.11766C>A MANE Select ENSP00000305941.3:p.Ala3922=
ENST00000674083.1:c.11766C>A ENSP00000501296.1:p.Ala3922=
ENST00000307340.7:c.11766C>A ENSP00000305941.3:p.Ala3922=
NM_206933.2:c.11766C>A NP_996816.2:p.Ala3922=
NM_206933.3:c.11766C>A NP_996816.2:p.Ala3922=
NM_206933.4:c.11766C>A MANE Select NP_996816.3:p.Ala3922=