Canonical Allele Identifier: CA2747719140
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215728496T>C , CM000663.2:g.215728496T>C GRCh38
NC_000001.10:g.215901838T>C , CM000663.1:g.215901838T>C GRCh37
NC_000001.9:g.213968461T>C NCBI36
NG_009497.1:g.699901A>G
NG_009497.2:g.699953A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.11712-112A>G MANE Select ENSP00000305941.3:n.11712-112A>G
ENST00000674083.1:c.11712-112A>G ENSP00000501296.1:n.11712-112A>G
ENST00000307340.7:c.11712-112A>G ENSP00000305941.3:n.11712-112A>G
NM_206933.2:c.11712-112A>G NP_996816.2:n.11712-112A>G
NM_206933.3:c.11712-112A>G NP_996816.2:n.11712-112A>G
NM_206933.4:c.11712-112A>G MANE Select NP_996816.3:n.11712-112A>G