Canonical Allele Identifier: CA344865714
Gene: USH2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.216247212G>T , CM000663.2:g.216247212G>T GRCh38
NC_000001.10:g.216420554G>T , CM000663.1:g.216420554G>T GRCh37
NC_000001.9:g.214487177G>T NCBI36
NG_009497.1:g.181185C>A
NG_009497.2:g.181237C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.2182C>A MANE Select ENSP00000305941.3:p.His728Asn
ENST00000674083.1:c.2182C>A ENSP00000501296.1:p.His728Asn
ENST00000307340.7:c.2182C>A ENSP00000305941.3:p.His728Asn
ENST00000366942.3:c.2182C>A ENSP00000355909.3:p.His728Asn
NM_007123.5:c.2182C>A NP_009054.5:p.His728Asn
NM_206933.2:c.2182C>A NP_996816.2:p.His728Asn
NM_206933.3:c.2182C>A NP_996816.2:p.His728Asn
NM_007123.6:c.2182C>A NP_009054.6:p.His728Asn
NM_206933.4:c.2182C>A MANE Select NP_996816.3:p.His728Asn