Canonical Allele Identifier: CA37459200
Gene: USH2A HGNC NCBI

Linked Data

dbSNP Id: rs374413719
gnomAD v3: 1-215866969-A-G
gnomAD v4: 1-215866969-A-G
MyVariant Identifiers: chr1:g.216040311A>G (hg19) chr1:g.215866969A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215866969A>G , CM000663.2:g.215866969A>G GRCh38
NC_000001.10:g.216040311A>G , CM000663.1:g.216040311A>G GRCh37
NC_000001.9:g.214106934A>G NCBI36
NG_009497.1:g.561428T>C
NG_009497.2:g.561480T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.8845+38T>C MANE Select ENSP00000305941.3:n.8845+38T>C
ENST00000674083.1:c.8845+38T>C ENSP00000501296.1:n.8845+38T>C
ENST00000307340.7:c.8845+38T>C ENSP00000305941.3:n.8845+38T>C
NM_206933.2:c.8845+38T>C NP_996816.2:n.8845+38T>C
NM_206933.3:c.8845+38T>C NP_996816.2:n.8845+38T>C
NM_206933.4:c.8845+38T>C MANE Select NP_996816.3:n.8845+38T>C
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