Canonical Allele Identifier: CA344850957
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 553940
ClinVar RCV Id: RCV000669486
dbSNP Id: rs1553270960

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215867017C>T , CM000663.2:g.215867017C>T GRCh38
NC_000001.10:g.216040359C>T , CM000663.1:g.216040359C>T GRCh37
NC_000001.9:g.214106982C>T NCBI36
NG_009497.1:g.561380G>A
NG_009497.2:g.561432G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.8835G>A MANE Select ENSP00000305941.3:p.Trp2945Ter
ENST00000674083.1:c.8835G>A ENSP00000501296.1:p.Trp2945Ter
ENST00000307340.7:c.8835G>A ENSP00000305941.3:p.Trp2945Ter
NM_206933.2:c.8835G>A NP_996816.2:p.Trp2945Ter
NM_206933.3:c.8835G>A NP_996816.2:p.Trp2945Ter
NM_206933.4:c.8835G>A MANE Select NP_996816.3:p.Trp2945Ter