Canonical Allele Identifier: CA423312993
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2756014
ClinVar RCV Id: RCV003571578
dbSNP Id: rs779661605
gnomAD v3: 1-215779970-C-T
gnomAD v4: 1-215779970-C-T
COSMIC: COSM425303 COSM4813800
MyVariant Identifiers: chr1:g.215953312C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215779970C>T , CM000663.2:g.215779970C>T GRCh38
NC_000001.10:g.215953312C>T , CM000663.1:g.215953312C>T GRCh37
NC_000001.9:g.214019935C>T NCBI36
NG_009497.1:g.648427G>A
NG_009497.2:g.648479G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.10812G>A MANE Select ENSP00000305941.3:p.Val3604=
ENST00000674083.1:c.10812G>A ENSP00000501296.1:p.Val3604=
ENST00000307340.7:c.10812G>A ENSP00000305941.3:p.Val3604=
NM_206933.2:c.10812G>A NP_996816.2:p.Val3604=
NM_206933.3:c.10812G>A NP_996816.2:p.Val3604=
NM_206933.4:c.10812G>A MANE Select NP_996816.3:p.Val3604=
Search 100 bp 5'
Search 100 bp 3'