Canonical Allele Identifier: CA1220455633
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215866968T= , CM000663.2:g.215866968T= GRCh38
NC_000001.10:g.216040310T= , CM000663.1:g.216040310T= GRCh37
NC_000001.9:g.214106933T= NCBI36
NG_009497.1:g.561429A=
NG_009497.2:g.561481A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.8845+39A= MANE Select ENSP00000305941.3:n.8845+39A=
ENST00000674083.1:c.8845+39A= ENSP00000501296.1:n.8845+39A=
ENST00000307340.7:c.8845+39A= ENSP00000305941.3:n.8845+39A=
NM_206933.2:c.8845+39A= NP_996816.2:n.8845+39A=
NM_206933.3:c.8845+39A= NP_996816.2:n.8845+39A=
NM_206933.4:c.8845+39A= MANE Select NP_996816.3:n.8845+39A=