Canonical Allele Identifier: CA423308866
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1653272
ClinVar RCV Id: RCV002160998
dbSNP Id: rs539877917
MyVariant Identifiers: chr1:g.215990441A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215817099A>C , CM000663.2:g.215817099A>C GRCh38
NC_000001.10:g.215990441A>C , CM000663.1:g.215990441A>C GRCh37
NC_000001.9:g.214057064A>C NCBI36
NG_009497.1:g.611298T>G
NG_009497.2:g.611350T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.9468T>G MANE Select ENSP00000305941.3:p.Thr3156=
ENST00000674083.1:c.9468T>G ENSP00000501296.1:p.Thr3156=
ENST00000307340.7:c.9468T>G ENSP00000305941.3:p.Thr3156=
NM_206933.2:c.9468T>G NP_996816.2:p.Thr3156=
NM_206933.3:c.9468T>G NP_996816.2:p.Thr3156=
NM_206933.4:c.9468T>G MANE Select NP_996816.3:p.Thr3156=
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