Canonical Allele Identifier: CA344825072
Gene: USH2A HGNC NCBI

Linked Data

dbSNP Id: rs1266573598

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215817119A>G , CM000663.2:g.215817119A>G GRCh38
NC_000001.10:g.215990461A>G , CM000663.1:g.215990461A>G GRCh37
NC_000001.9:g.214057084A>G NCBI36
NG_009497.1:g.611278T>C
NG_009497.2:g.611330T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.9448T>C MANE Select ENSP00000305941.3:p.Trp3150Arg
ENST00000674083.1:c.9448T>C ENSP00000501296.1:p.Trp3150Arg
ENST00000307340.7:c.9448T>C ENSP00000305941.3:p.Trp3150Arg
NM_206933.2:c.9448T>C NP_996816.2:p.Trp3150Arg
NM_206933.3:c.9448T>C NP_996816.2:p.Trp3150Arg
NM_206933.4:c.9448T>C MANE Select NP_996816.3:p.Trp3150Arg