Canonical Allele Identifier: CA344833341
Gene: USH2A HGNC NCBI

Linked Data

dbSNP Id: rs1246794638

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215779884A>G , CM000663.2:g.215779884A>G GRCh38
NC_000001.10:g.215953226A>G , CM000663.1:g.215953226A>G GRCh37
NC_000001.9:g.214019849A>G NCBI36
NG_009497.1:g.648513T>C
NG_009497.2:g.648565T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.10898T>C MANE Select ENSP00000305941.3:p.Ile3633Thr
ENST00000674083.1:c.10898T>C ENSP00000501296.1:p.Ile3633Thr
ENST00000307340.7:c.10898T>C ENSP00000305941.3:p.Ile3633Thr
NM_206933.2:c.10898T>C NP_996816.2:p.Ile3633Thr
NM_206933.3:c.10898T>C NP_996816.2:p.Ile3633Thr
NM_206933.4:c.10898T>C MANE Select NP_996816.3:p.Ile3633Thr