Canonical Allele Identifier: CA1393911
Gene: USH2A HGNC NCBI

Linked Data

dbSNP Id: rs764267390
ExAC: 1:215953296 A / G
gnomAD v4: 1-215779954-A-G
MyVariant Identifiers: chr1:g.215953296A>G (hg19) chr1:g.215779954A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215779954A>G , CM000663.2:g.215779954A>G GRCh38
NC_000001.10:g.215953296A>G , CM000663.1:g.215953296A>G GRCh37
NC_000001.9:g.214019919A>G NCBI36
NG_009497.1:g.648443T>C
NG_009497.2:g.648495T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000307340.8:c.10828T>C MANE Select ENSP00000305941.3:p.Trp3610Arg
ENST00000674083.1:c.10828T>C ENSP00000501296.1:p.Trp3610Arg
ENST00000307340.7:c.10828T>C ENSP00000305941.3:p.Trp3610Arg
NM_206933.2:c.10828T>C NP_996816.2:p.Trp3610Arg
NM_206933.3:c.10828T>C NP_996816.2:p.Trp3610Arg
NM_206933.4:c.10828T>C MANE Select NP_996816.3:p.Trp3610Arg
Search 100 bp 5'
Search 100 bp 3'