Canonical Allele Identifier: CA1220446642
Gene: USH2A HGNC NCBI

Linked Data

dbSNP Id: rs1663822297

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215845750A>C , CM000663.2:g.215845750A>C GRCh38
NC_000001.10:g.216019092A>C , CM000663.1:g.216019092A>C GRCh37
NC_000001.9:g.214085715A>C NCBI36
NG_009497.1:g.582647T>G
NG_009497.2:g.582699T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.9055+74T>G MANE Select ENSP00000305941.3:n.9055+74T>G
ENST00000674083.1:c.9055+74T>G ENSP00000501296.1:n.9055+74T>G
ENST00000307340.7:c.9055+74T>G ENSP00000305941.3:n.9055+74T>G
NM_206933.2:c.9055+74T>G NP_996816.2:n.9055+74T>G
NM_206933.3:c.9055+74T>G NP_996816.2:n.9055+74T>G
NM_206933.4:c.9055+74T>G MANE Select NP_996816.3:n.9055+74T>G