Canonical Allele Identifier: CA1146271469
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215866950A= , CM000663.2:g.215866950A= GRCh38
NC_000001.10:g.216040292A= , CM000663.1:g.216040292A= GRCh37
NC_000001.9:g.214106915A= NCBI36
NG_009497.1:g.561447T=
NG_009497.2:g.561499T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.8845+57T= MANE Select ENSP00000305941.3:n.8845+57T=
ENST00000674083.1:c.8845+57T= ENSP00000501296.1:n.8845+57T=
ENST00000307340.7:c.8845+57T= ENSP00000305941.3:n.8845+57T=
NM_206933.2:c.8845+57T= NP_996816.2:n.8845+57T=
NM_206933.3:c.8845+57T= NP_996816.2:n.8845+57T=
NM_206933.4:c.8845+57T= MANE Select NP_996816.3:n.8845+57T=