Canonical Allele Identifier: CA344833169
Gene: USH2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215779867C>A , CM000663.2:g.215779867C>A GRCh38
NC_000001.10:g.215953209C>A , CM000663.1:g.215953209C>A GRCh37
NC_000001.9:g.214019832C>A NCBI36
NG_009497.1:g.648530G>T
NG_009497.2:g.648582G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.10915G>T MANE Select ENSP00000305941.3:p.Asp3639Tyr
ENST00000674083.1:c.10915G>T ENSP00000501296.1:p.Asp3639Tyr
ENST00000307340.7:c.10915G>T ENSP00000305941.3:p.Asp3639Tyr
NM_206933.2:c.10915G>T NP_996816.2:p.Asp3639Tyr
NM_206933.3:c.10915G>T NP_996816.2:p.Asp3639Tyr
NM_206933.4:c.10915G>T MANE Select NP_996816.3:p.Asp3639Tyr